Canonical Allele Identifier: CA1188179402
Gene: AMPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628719A= , CM000663.2:g.109628719A= GRCh38
NC_000001.10:g.110171341A= , CM000663.1:g.110171341A= GRCh37
NC_000001.9:g.109972864A= NCBI36
NG_034075.1:g.13907A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1484A= ENSP00000256578.4:p.Asp495=
ENST00000358729.9:c.1484A= ENSP00000351573.5:p.Asp495=
ENST00000369840.7:c.1484A= ENSP00000358855.3:p.Asp495=
ENST00000474459.6:n.2103A=
ENST00000476688.3:c.1166A= ENSP00000437025.2:p.Asp389=
ENST00000486282.7:n.2440A=
ENST00000524975.2:n.1965A=
ENST00000525415.2:n.2000A=
ENST00000526301.6:n.1547A=
ENST00000527846.7:n.1339A=
ENST00000528667.7:c.1484A= MANE Select ENSP00000436541.2:p.Asp495=
ENST00000531203.6:c.1292A= ENSP00000431975.2:p.Asp431=
ENST00000531734.6:c.1403A= ENSP00000433739.2:p.Asp468=
ENST00000652975.2:c.*1236A= ENSP00000499620.2:n.*1236A=
ENST00000654851.1:n.1326A=
ENST00000655992.1:c.1292A= ENSP00000499740.1:p.Asp431=
ENST00000659122.2:c.1407+224A= ENSP00000499621.2:n.1407+224A=
ENST00000663749.1:c.*1231A= ENSP00000499739.1:n.*1231A=
ENST00000667949.2:c.884A= ENSP00000499465.2:p.Asp295=
ENST00000668421.1:c.*1425A= ENSP00000499362.1:n.*1425A=
ENST00000679379.1:c.*1236A= ENSP00000505528.1:n.*1236A=
ENST00000679593.1:c.1484A= ENSP00000505999.1:p.Asp495=
ENST00000679880.1:n.2020A=
ENST00000679892.1:c.*1252A= ENSP00000504882.1:n.*1252A=
ENST00000679981.1:c.*1498A= ENSP00000506422.1:n.*1498A=
ENST00000680132.1:c.*1434A= ENSP00000505950.1:n.*1434A=
ENST00000680148.1:c.*1236A= ENSP00000505994.1:n.*1236A=
ENST00000680170.1:n.2349A=
ENST00000680192.1:n.2442A=
ENST00000680519.1:n.1720A=
ENST00000680531.1:c.*1231A= ENSP00000506332.1:n.*1231A=
ENST00000680820.1:c.*1236A= ENSP00000505735.1:n.*1236A=
ENST00000680832.1:c.*1584A= ENSP00000505774.1:n.*1584A=
ENST00000680929.1:c.*1173A= ENSP00000504916.1:n.*1173A=
ENST00000681108.1:c.*1245+224A= ENSP00000506701.1:n.*1245+224A=
ENST00000681121.1:c.*594A= ENSP00000506466.1:n.*594A=
ENST00000681132.1:c.*1250A= ENSP00000506195.1:n.*1250A=
ENST00000681181.1:c.*1469A= ENSP00000506038.1:n.*1469A=
ENST00000681218.1:c.*1757A= ENSP00000505976.1:n.*1757A=
ENST00000681246.1:c.*1140A= ENSP00000505534.1:n.*1140A=
ENST00000681496.1:c.*1757A= ENSP00000505948.1:n.*1757A=
ENST00000681834.1:n.1823A=
ENST00000681862.1:c.*1610A= ENSP00000505537.1:n.*1610A=
ENST00000256578.7:c.1646A= ENSP00000256578.3:p.Asp549=
ENST00000342115.8:c.1403A= ENSP00000345498.4:p.Asp468=
ENST00000358729.8:c.1421A= ENSP00000351573.4:p.Asp474=
ENST00000369840.6:c.1557A=
ENST00000393688.7:c.1289A= ENSP00000377292.3:p.Asp430=
ENST00000467071.1:n.6A=
ENST00000526301.5:n.1685A=
ENST00000528454.5:c.1292A= ENSP00000437164.1:p.Asp431=
ENST00000528667.5:c.1646A= ENSP00000436541.1:p.Asp549=
ENST00000532851.1:n.194A=
ENST00000533132.1:n.186A=
NM_001257360.1:c.1646A= NP_001244289.1:p.Asp549=
NM_001257361.1:c.1292A= NP_001244290.1:p.Asp431=
NM_001308170.1:c.1421A= NP_001295099.1:p.Asp474=
NM_004037.7:c.1646A= NP_004028.3:p.Asp549=
NM_139156.3:c.1403A= NP_631895.1:p.Asp468=
NM_203404.1:c.1289A= NP_981949.1:p.Asp430=
XM_011541247.1:c.1859A= XP_011539549.1:p.Asp620=
XM_011541248.1:c.1782+224A= XP_011539550.1:n.1782+224A=
XR_946607.1:n.1882A=
XM_024446431.1:c.1421A= XP_024302199.1:p.Asp474=
XM_024446432.1:c.1430+224A= XP_024302200.1:n.1430+224A=
XR_002956282.1:n.2057A=
NM_001257360.2:c.1646A= NP_001244289.1:p.Asp549=
NM_001368809.2:c.1484A= MANE Select NP_001355738.1:p.Asp495=
NM_004037.9:c.1484A= NP_004028.4:p.Asp495=
NM_001257361.2:c.1292A= NP_001244290.1:p.Asp431=
NM_139156.4:c.1403A= NP_631895.1:p.Asp468=