Canonical Allele Identifier: CA1188179388
Gene: AMPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628685G= , CM000663.2:g.109628685G= GRCh38
NC_000001.10:g.110171307G= , CM000663.1:g.110171307G= GRCh37
NC_000001.9:g.109972830G= NCBI36
NG_034075.1:g.13873G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1450G= ENSP00000256578.4:p.Glu484=
ENST00000358729.9:c.1450G= ENSP00000351573.5:p.Glu484=
ENST00000369840.7:c.1450G= ENSP00000358855.3:p.Glu484=
ENST00000474459.6:n.2069G=
ENST00000476688.3:c.1132G= ENSP00000437025.2:p.Glu378=
ENST00000486282.7:n.2406G=
ENST00000524975.2:n.1931G=
ENST00000525415.2:n.1966G=
ENST00000526301.6:n.1513G=
ENST00000527846.7:n.1305G=
ENST00000528667.7:c.1450G= MANE Select ENSP00000436541.2:p.Glu484=
ENST00000531203.6:c.1258G= ENSP00000431975.2:p.Glu420=
ENST00000531734.6:c.1369G= ENSP00000433739.2:p.Glu457=
ENST00000652975.2:c.*1202G= ENSP00000499620.2:n.*1202G=
ENST00000654851.1:n.1292G=
ENST00000655992.1:c.1258G= ENSP00000499740.1:p.Glu420=
ENST00000659122.2:c.1407+190G= ENSP00000499621.2:n.1407+190G=
ENST00000663749.1:c.*1197G= ENSP00000499739.1:n.*1197G=
ENST00000667949.2:c.850G= ENSP00000499465.2:p.Glu284=
ENST00000668421.1:c.*1391G= ENSP00000499362.1:n.*1391G=
ENST00000679379.1:c.*1202G= ENSP00000505528.1:n.*1202G=
ENST00000679593.1:c.1450G= ENSP00000505999.1:p.Glu484=
ENST00000679880.1:n.1986G=
ENST00000679892.1:c.*1218G= ENSP00000504882.1:n.*1218G=
ENST00000679981.1:c.*1464G= ENSP00000506422.1:n.*1464G=
ENST00000680132.1:c.*1400G= ENSP00000505950.1:n.*1400G=
ENST00000680148.1:c.*1202G= ENSP00000505994.1:n.*1202G=
ENST00000680170.1:n.2315G=
ENST00000680192.1:n.2408G=
ENST00000680519.1:n.1686G=
ENST00000680531.1:c.*1197G= ENSP00000506332.1:n.*1197G=
ENST00000680820.1:c.*1202G= ENSP00000505735.1:n.*1202G=
ENST00000680832.1:c.*1550G= ENSP00000505774.1:n.*1550G=
ENST00000680929.1:c.*1139G= ENSP00000504916.1:n.*1139G=
ENST00000681108.1:c.*1245+190G= ENSP00000506701.1:n.*1245+190G=
ENST00000681121.1:c.*560G= ENSP00000506466.1:n.*560G=
ENST00000681132.1:c.*1216G= ENSP00000506195.1:n.*1216G=
ENST00000681181.1:c.*1435G= ENSP00000506038.1:n.*1435G=
ENST00000681218.1:c.*1723G= ENSP00000505976.1:n.*1723G=
ENST00000681246.1:c.*1106G= ENSP00000505534.1:n.*1106G=
ENST00000681496.1:c.*1723G= ENSP00000505948.1:n.*1723G=
ENST00000681834.1:n.1789G=
ENST00000681862.1:c.*1576G= ENSP00000505537.1:n.*1576G=
ENST00000256578.7:c.1612G= ENSP00000256578.3:p.Glu538=
ENST00000342115.8:c.1369G= ENSP00000345498.4:p.Glu457=
ENST00000358729.8:c.1387G= ENSP00000351573.4:p.Glu463=
ENST00000369840.6:c.1523G=
ENST00000393688.7:c.1255G= ENSP00000377292.3:p.Glu419=
ENST00000526301.5:n.1651G=
ENST00000528454.5:c.1258G= ENSP00000437164.1:p.Glu420=
ENST00000528667.5:c.1612G= ENSP00000436541.1:p.Glu538=
ENST00000532851.1:n.160G=
ENST00000533132.1:n.152G=
NM_001257360.1:c.1612G= NP_001244289.1:p.Glu538=
NM_001257361.1:c.1258G= NP_001244290.1:p.Glu420=
NM_001308170.1:c.1387G= NP_001295099.1:p.Glu463=
NM_004037.7:c.1612G= NP_004028.3:p.Glu538=
NM_139156.3:c.1369G= NP_631895.1:p.Glu457=
NM_203404.1:c.1255G= NP_981949.1:p.Glu419=
XM_011541247.1:c.1825G= XP_011539549.1:p.Glu609=
XM_011541248.1:c.1782+190G= XP_011539550.1:n.1782+190G=
XR_946607.1:n.1848G=
XM_024446431.1:c.1387G= XP_024302199.1:p.Glu463=
XM_024446432.1:c.1430+190G= XP_024302200.1:n.1430+190G=
XR_002956282.1:n.2023G=
NM_001257360.2:c.1612G= NP_001244289.1:p.Glu538=
NM_001368809.2:c.1450G= MANE Select NP_001355738.1:p.Glu484=
NM_004037.9:c.1450G= NP_004028.4:p.Glu484=
NM_001257361.2:c.1258G= NP_001244290.1:p.Glu420=
NM_139156.4:c.1369G= NP_631895.1:p.Glu457=