Canonical Allele Identifier: CA1147557321
Gene: AMPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628657C= , CM000663.2:g.109628657C= GRCh38
NC_000001.10:g.110171279C= , CM000663.1:g.110171279C= GRCh37
NC_000001.9:g.109972802C= NCBI36
NG_034075.1:g.13845C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1422C= ENSP00000256578.4:p.Asp474=
ENST00000358729.9:c.1422C= ENSP00000351573.5:p.Asp474=
ENST00000369840.7:c.1422C= ENSP00000358855.3:p.Asp474=
ENST00000474459.6:n.2041C=
ENST00000476688.3:c.1104C= ENSP00000437025.2:p.Asp368=
ENST00000486282.7:n.2378C=
ENST00000524975.2:n.1903C=
ENST00000525415.2:n.1938C=
ENST00000526301.6:n.1485C=
ENST00000527846.7:n.1277C=
ENST00000528667.7:c.1422C= MANE Select ENSP00000436541.2:p.Asp474=
ENST00000531203.6:c.1230C= ENSP00000431975.2:p.Asp410=
ENST00000531734.6:c.1341C= ENSP00000433739.2:p.Asp447=
ENST00000652975.2:c.*1174C= ENSP00000499620.2:n.*1174C=
ENST00000654851.1:n.1264C=
ENST00000655992.1:c.1230C= ENSP00000499740.1:p.Asp410=
ENST00000659122.2:c.1407+162C= ENSP00000499621.2:n.1407+162C=
ENST00000663749.1:c.*1169C= ENSP00000499739.1:n.*1169C=
ENST00000667949.2:c.822C= ENSP00000499465.2:p.Asp274=
ENST00000668421.1:c.*1363C= ENSP00000499362.1:n.*1363C=
ENST00000679379.1:c.*1174C= ENSP00000505528.1:n.*1174C=
ENST00000679593.1:c.1422C= ENSP00000505999.1:p.Asp474=
ENST00000679880.1:n.1958C=
ENST00000679892.1:c.*1190C= ENSP00000504882.1:n.*1190C=
ENST00000679981.1:c.*1436C= ENSP00000506422.1:n.*1436C=
ENST00000680132.1:c.*1372C= ENSP00000505950.1:n.*1372C=
ENST00000680148.1:c.*1174C= ENSP00000505994.1:n.*1174C=
ENST00000680170.1:n.2287C=
ENST00000680192.1:n.2380C=
ENST00000680519.1:n.1658C=
ENST00000680531.1:c.*1169C= ENSP00000506332.1:n.*1169C=
ENST00000680820.1:c.*1174C= ENSP00000505735.1:n.*1174C=
ENST00000680832.1:c.*1522C= ENSP00000505774.1:n.*1522C=
ENST00000680929.1:c.*1111C= ENSP00000504916.1:n.*1111C=
ENST00000681108.1:c.*1245+162C= ENSP00000506701.1:n.*1245+162C=
ENST00000681121.1:c.*532C= ENSP00000506466.1:n.*532C=
ENST00000681132.1:c.*1188C= ENSP00000506195.1:n.*1188C=
ENST00000681181.1:c.*1407C= ENSP00000506038.1:n.*1407C=
ENST00000681218.1:c.*1695C= ENSP00000505976.1:n.*1695C=
ENST00000681246.1:c.*1078C= ENSP00000505534.1:n.*1078C=
ENST00000681496.1:c.*1695C= ENSP00000505948.1:n.*1695C=
ENST00000681834.1:n.1761C=
ENST00000681862.1:c.*1548C= ENSP00000505537.1:n.*1548C=
ENST00000256578.7:c.1584C= ENSP00000256578.3:p.Asp528=
ENST00000342115.8:c.1341C= ENSP00000345498.4:p.Asp447=
ENST00000358729.8:c.1359C= ENSP00000351573.4:p.Asp453=
ENST00000369840.6:c.1495C=
ENST00000393688.7:c.1227C= ENSP00000377292.3:p.Asp409=
ENST00000526301.5:n.1623C=
ENST00000528454.5:c.1230C= ENSP00000437164.1:p.Asp410=
ENST00000528667.5:c.1584C= ENSP00000436541.1:p.Asp528=
ENST00000532851.1:n.132C=
ENST00000533132.1:n.124C=
NM_001257360.1:c.1584C= NP_001244289.1:p.Asp528=
NM_001257361.1:c.1230C= NP_001244290.1:p.Asp410=
NM_001308170.1:c.1359C= NP_001295099.1:p.Asp453=
NM_004037.7:c.1584C= NP_004028.3:p.Asp528=
NM_139156.3:c.1341C= NP_631895.1:p.Asp447=
NM_203404.1:c.1227C= NP_981949.1:p.Asp409=
XM_011541247.1:c.1797C= XP_011539549.1:p.Asp599=
XM_011541248.1:c.1782+162C= XP_011539550.1:n.1782+162C=
XR_946607.1:n.1820C=
XM_024446431.1:c.1359C= XP_024302199.1:p.Asp453=
XM_024446432.1:c.1430+162C= XP_024302200.1:n.1430+162C=
XR_002956282.1:n.1995C=
NM_001257360.2:c.1584C= NP_001244289.1:p.Asp528=
NM_001368809.2:c.1422C= MANE Select NP_001355738.1:p.Asp474=
NM_004037.9:c.1422C= NP_004028.4:p.Asp474=
NM_001257361.2:c.1230C= NP_001244290.1:p.Asp410=
NM_139156.4:c.1341C= NP_631895.1:p.Asp447=