Canonical Allele Identifier: CA1188179385
Gene: AMPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628673T= , CM000663.2:g.109628673T= GRCh38
NC_000001.10:g.110171295T= , CM000663.1:g.110171295T= GRCh37
NC_000001.9:g.109972818T= NCBI36
NG_034075.1:g.13861T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1438T= ENSP00000256578.4:p.Tyr480=
ENST00000358729.9:c.1438T= ENSP00000351573.5:p.Tyr480=
ENST00000369840.7:c.1438T= ENSP00000358855.3:p.Tyr480=
ENST00000474459.6:n.2057T=
ENST00000476688.3:c.1120T= ENSP00000437025.2:p.Tyr374=
ENST00000486282.7:n.2394T=
ENST00000524975.2:n.1919T=
ENST00000525415.2:n.1954T=
ENST00000526301.6:n.1501T=
ENST00000527846.7:n.1293T=
ENST00000528667.7:c.1438T= MANE Select ENSP00000436541.2:p.Tyr480=
ENST00000531203.6:c.1246T= ENSP00000431975.2:p.Tyr416=
ENST00000531734.6:c.1357T= ENSP00000433739.2:p.Tyr453=
ENST00000652975.2:c.*1190T= ENSP00000499620.2:n.*1190T=
ENST00000654851.1:n.1280T=
ENST00000655992.1:c.1246T= ENSP00000499740.1:p.Tyr416=
ENST00000659122.2:c.1407+178T= ENSP00000499621.2:n.1407+178T=
ENST00000663749.1:c.*1185T= ENSP00000499739.1:n.*1185T=
ENST00000667949.2:c.838T= ENSP00000499465.2:p.Tyr280=
ENST00000668421.1:c.*1379T= ENSP00000499362.1:n.*1379T=
ENST00000679379.1:c.*1190T= ENSP00000505528.1:n.*1190T=
ENST00000679593.1:c.1438T= ENSP00000505999.1:p.Tyr480=
ENST00000679880.1:n.1974T=
ENST00000679892.1:c.*1206T= ENSP00000504882.1:n.*1206T=
ENST00000679981.1:c.*1452T= ENSP00000506422.1:n.*1452T=
ENST00000680132.1:c.*1388T= ENSP00000505950.1:n.*1388T=
ENST00000680148.1:c.*1190T= ENSP00000505994.1:n.*1190T=
ENST00000680170.1:n.2303T=
ENST00000680192.1:n.2396T=
ENST00000680519.1:n.1674T=
ENST00000680531.1:c.*1185T= ENSP00000506332.1:n.*1185T=
ENST00000680820.1:c.*1190T= ENSP00000505735.1:n.*1190T=
ENST00000680832.1:c.*1538T= ENSP00000505774.1:n.*1538T=
ENST00000680929.1:c.*1127T= ENSP00000504916.1:n.*1127T=
ENST00000681108.1:c.*1245+178T= ENSP00000506701.1:n.*1245+178T=
ENST00000681121.1:c.*548T= ENSP00000506466.1:n.*548T=
ENST00000681132.1:c.*1204T= ENSP00000506195.1:n.*1204T=
ENST00000681181.1:c.*1423T= ENSP00000506038.1:n.*1423T=
ENST00000681218.1:c.*1711T= ENSP00000505976.1:n.*1711T=
ENST00000681246.1:c.*1094T= ENSP00000505534.1:n.*1094T=
ENST00000681496.1:c.*1711T= ENSP00000505948.1:n.*1711T=
ENST00000681834.1:n.1777T=
ENST00000681862.1:c.*1564T= ENSP00000505537.1:n.*1564T=
ENST00000256578.7:c.1600T= ENSP00000256578.3:p.Tyr534=
ENST00000342115.8:c.1357T= ENSP00000345498.4:p.Tyr453=
ENST00000358729.8:c.1375T= ENSP00000351573.4:p.Tyr459=
ENST00000369840.6:c.1511T=
ENST00000393688.7:c.1243T= ENSP00000377292.3:p.Tyr415=
ENST00000526301.5:n.1639T=
ENST00000528454.5:c.1246T= ENSP00000437164.1:p.Tyr416=
ENST00000528667.5:c.1600T= ENSP00000436541.1:p.Tyr534=
ENST00000532851.1:n.148T=
ENST00000533132.1:n.140T=
NM_001257360.1:c.1600T= NP_001244289.1:p.Tyr534=
NM_001257361.1:c.1246T= NP_001244290.1:p.Tyr416=
NM_001308170.1:c.1375T= NP_001295099.1:p.Tyr459=
NM_004037.7:c.1600T= NP_004028.3:p.Tyr534=
NM_139156.3:c.1357T= NP_631895.1:p.Tyr453=
NM_203404.1:c.1243T= NP_981949.1:p.Tyr415=
XM_011541247.1:c.1813T= XP_011539549.1:p.Tyr605=
XM_011541248.1:c.1782+178T= XP_011539550.1:n.1782+178T=
XR_946607.1:n.1836T=
XM_024446431.1:c.1375T= XP_024302199.1:p.Tyr459=
XM_024446432.1:c.1430+178T= XP_024302200.1:n.1430+178T=
XR_002956282.1:n.2011T=
NM_001257360.2:c.1600T= NP_001244289.1:p.Tyr534=
NM_001368809.2:c.1438T= MANE Select NP_001355738.1:p.Tyr480=
NM_004037.9:c.1438T= NP_004028.4:p.Tyr480=
NM_001257361.2:c.1246T= NP_001244290.1:p.Tyr416=
NM_139156.4:c.1357T= NP_631895.1:p.Tyr453=