Canonical Allele Identifier: CA1188179403
Gene: AMPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628724_109628725delinsTG , CM000663.2:g.109628724_109628725delinsTG GRCh38
NC_000001.10:g.110171346_110171347delinsTG , CM000663.1:g.110171346_110171347delinsTG GRCh37
NC_000001.9:g.109972869_109972870delinsTG NCBI36
NG_034075.1:g.13912_13913delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1489_1490delinsTG ENSP00000256578.4:p.Trp497=
ENST00000358729.9:c.1489_1490delinsTG ENSP00000351573.5:p.Trp497=
ENST00000369840.7:c.1489_1490delinsTG ENSP00000358855.3:p.Trp497=
ENST00000474459.6:n.2108_2109delinsTG
ENST00000476688.3:c.1171_1172delinsTG ENSP00000437025.2:p.Trp391=
ENST00000486282.7:n.2445_2446delinsTG
ENST00000524975.2:n.1970_1971delinsTG
ENST00000525415.2:n.2005_2006delinsTG
ENST00000526301.6:n.1552_1553delinsTG
ENST00000527846.7:n.1344_1345delinsTG
ENST00000528667.7:c.1489_1490delinsTG MANE Select ENSP00000436541.2:p.Trp497=
ENST00000531203.6:c.1297_1298delinsTG ENSP00000431975.2:p.Trp433=
ENST00000531734.6:c.1408_1409delinsTG ENSP00000433739.2:p.Trp470=
ENST00000652975.2:c.*1241_*1242delinsTG ENSP00000499620.2:n.*1241_*1242delinsTG
ENST00000654851.1:n.1331_1332delinsTG
ENST00000655992.1:c.1297_1298delinsTG ENSP00000499740.1:p.Trp433=
ENST00000659122.2:c.1407+229_1407+230delinsTG ENSP00000499621.2:n.1407+229_1407+230delinsTG
ENST00000663749.1:c.*1236_*1237delinsTG ENSP00000499739.1:n.*1236_*1237delinsTG
ENST00000667949.2:c.889_890delinsTG ENSP00000499465.2:p.Trp297=
ENST00000668421.1:c.*1430_*1431delinsTG ENSP00000499362.1:n.*1430_*1431delinsTG
ENST00000679379.1:c.*1241_*1242delinsTG ENSP00000505528.1:n.*1241_*1242delinsTG
ENST00000679593.1:c.1489_1490delinsTG ENSP00000505999.1:p.Trp497=
ENST00000679880.1:n.2025_2026delinsTG
ENST00000679892.1:c.*1257_*1258delinsTG ENSP00000504882.1:n.*1257_*1258delinsTG
ENST00000679981.1:c.*1503_*1504delinsTG ENSP00000506422.1:n.*1503_*1504delinsTG
ENST00000680132.1:c.*1439_*1440delinsTG ENSP00000505950.1:n.*1439_*1440delinsTG
ENST00000680148.1:c.*1241_*1242delinsTG ENSP00000505994.1:n.*1241_*1242delinsTG
ENST00000680170.1:n.2354_2355delinsTG
ENST00000680192.1:n.2447_2448delinsTG
ENST00000680519.1:n.1725_1726delinsTG
ENST00000680531.1:c.*1236_*1237delinsTG ENSP00000506332.1:n.*1236_*1237delinsTG
ENST00000680820.1:c.*1241_*1242delinsTG ENSP00000505735.1:n.*1241_*1242delinsTG
ENST00000680832.1:c.*1589_*1590delinsTG ENSP00000505774.1:n.*1589_*1590delinsTG
ENST00000680929.1:c.*1178_*1179delinsTG ENSP00000504916.1:n.*1178_*1179delinsTG
ENST00000681108.1:c.*1245+229_*1245+230delinsTG ENSP00000506701.1:n.*1245+229_*1245+230delinsTG
ENST00000681121.1:c.*599_*600delinsTG ENSP00000506466.1:n.*599_*600delinsTG
ENST00000681132.1:c.*1255_*1256delinsTG ENSP00000506195.1:n.*1255_*1256delinsTG
ENST00000681181.1:c.*1474_*1475delinsTG ENSP00000506038.1:n.*1474_*1475delinsTG
ENST00000681218.1:c.*1762_*1763delinsTG ENSP00000505976.1:n.*1762_*1763delinsTG
ENST00000681246.1:c.*1145_*1146delinsTG ENSP00000505534.1:n.*1145_*1146delinsTG
ENST00000681496.1:c.*1762_*1763delinsTG ENSP00000505948.1:n.*1762_*1763delinsTG
ENST00000681834.1:n.1828_1829delinsTG
ENST00000681862.1:c.*1615_*1616delinsTG ENSP00000505537.1:n.*1615_*1616delinsTG
ENST00000256578.7:c.1651_1652delinsTG ENSP00000256578.3:p.Trp551=
ENST00000342115.8:c.1408_1409delinsTG ENSP00000345498.4:p.Trp470=
ENST00000358729.8:c.1426_1427delinsTG ENSP00000351573.4:p.Trp476=
ENST00000369840.6:c.1562_1563delinsTG
ENST00000393688.7:c.1294_1295delinsTG ENSP00000377292.3:p.Trp432=
ENST00000467071.1:n.11_12delinsTG
ENST00000526301.5:n.1690_1691delinsTG
ENST00000528454.5:c.1297_1298delinsTG ENSP00000437164.1:p.Trp433=
ENST00000528667.5:c.1651_1652delinsTG ENSP00000436541.1:p.Trp551=
ENST00000532851.1:n.199_200delinsTG
ENST00000533132.1:n.191_192delinsTG
NM_001257360.1:c.1651_1652delinsTG NP_001244289.1:p.Trp551=
NM_001257361.1:c.1297_1298delinsTG NP_001244290.1:p.Trp433=
NM_001308170.1:c.1426_1427delinsTG NP_001295099.1:p.Trp476=
NM_004037.7:c.1651_1652delinsTG NP_004028.3:p.Trp551=
NM_139156.3:c.1408_1409delinsTG NP_631895.1:p.Trp470=
NM_203404.1:c.1294_1295delinsTG NP_981949.1:p.Trp432=
XM_011541247.1:c.1864_1865delinsTG XP_011539549.1:p.Trp622=
XM_011541248.1:c.1782+229_1782+230delinsTG XP_011539550.1:n.1782+229_1782+230delinsTG
XR_946607.1:n.1887_1888delinsTG
XM_024446431.1:c.1426_1427delinsTG XP_024302199.1:p.Trp476=
XM_024446432.1:c.1430+229_1430+230delinsTG XP_024302200.1:n.1430+229_1430+230delinsTG
XR_002956282.1:n.2062_2063delinsTG
NM_001257360.2:c.1651_1652delinsTG NP_001244289.1:p.Trp551=
NM_001368809.2:c.1489_1490delinsTG MANE Select NP_001355738.1:p.Trp497=
NM_004037.9:c.1489_1490delinsTG NP_004028.4:p.Trp497=
NM_001257361.2:c.1297_1298delinsTG NP_001244290.1:p.Trp433=
NM_139156.4:c.1408_1409delinsTG NP_631895.1:p.Trp470=