Canonical Allele Identifier: CA419684894
Gene: AMPD2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.110171315G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628693G>A , CM000663.2:g.109628693G>A GRCh38
NC_000001.10:g.110171315G>A , CM000663.1:g.110171315G>A GRCh37
NC_000001.9:g.109972838G>A NCBI36
NG_034075.1:g.13881G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1458G>A ENSP00000256578.4:p.Arg486=
ENST00000358729.9:c.1458G>A ENSP00000351573.5:p.Arg486=
ENST00000369840.7:c.1458G>A ENSP00000358855.3:p.Arg486=
ENST00000474459.6:n.2077G>A
ENST00000476688.3:c.1140G>A ENSP00000437025.2:p.Arg380=
ENST00000486282.7:n.2414G>A
ENST00000524975.2:n.1939G>A
ENST00000525415.2:n.1974G>A
ENST00000526301.6:n.1521G>A
ENST00000527846.7:n.1313G>A
ENST00000528667.7:c.1458G>A MANE Select ENSP00000436541.2:p.Arg486=
ENST00000531203.6:c.1266G>A ENSP00000431975.2:p.Arg422=
ENST00000531734.6:c.1377G>A ENSP00000433739.2:p.Arg459=
ENST00000652975.2:c.*1210G>A ENSP00000499620.2:n.*1210G>A
ENST00000654851.1:n.1300G>A
ENST00000655992.1:c.1266G>A ENSP00000499740.1:p.Arg422=
ENST00000659122.2:c.1407+198G>A ENSP00000499621.2:n.1407+198G>A
ENST00000663749.1:c.*1205G>A ENSP00000499739.1:n.*1205G>A
ENST00000667949.2:c.858G>A ENSP00000499465.2:p.Arg286=
ENST00000668421.1:c.*1399G>A ENSP00000499362.1:n.*1399G>A
ENST00000679379.1:c.*1210G>A ENSP00000505528.1:n.*1210G>A
ENST00000679593.1:c.1458G>A ENSP00000505999.1:p.Arg486=
ENST00000679880.1:n.1994G>A
ENST00000679892.1:c.*1226G>A ENSP00000504882.1:n.*1226G>A
ENST00000679981.1:c.*1472G>A ENSP00000506422.1:n.*1472G>A
ENST00000680132.1:c.*1408G>A ENSP00000505950.1:n.*1408G>A
ENST00000680148.1:c.*1210G>A ENSP00000505994.1:n.*1210G>A
ENST00000680170.1:n.2323G>A
ENST00000680192.1:n.2416G>A
ENST00000680519.1:n.1694G>A
ENST00000680531.1:c.*1205G>A ENSP00000506332.1:n.*1205G>A
ENST00000680820.1:c.*1210G>A ENSP00000505735.1:n.*1210G>A
ENST00000680832.1:c.*1558G>A ENSP00000505774.1:n.*1558G>A
ENST00000680929.1:c.*1147G>A ENSP00000504916.1:n.*1147G>A
ENST00000681108.1:c.*1245+198G>A ENSP00000506701.1:n.*1245+198G>A
ENST00000681121.1:c.*568G>A ENSP00000506466.1:n.*568G>A
ENST00000681132.1:c.*1224G>A ENSP00000506195.1:n.*1224G>A
ENST00000681181.1:c.*1443G>A ENSP00000506038.1:n.*1443G>A
ENST00000681218.1:c.*1731G>A ENSP00000505976.1:n.*1731G>A
ENST00000681246.1:c.*1114G>A ENSP00000505534.1:n.*1114G>A
ENST00000681496.1:c.*1731G>A ENSP00000505948.1:n.*1731G>A
ENST00000681834.1:n.1797G>A
ENST00000681862.1:c.*1584G>A ENSP00000505537.1:n.*1584G>A
ENST00000256578.7:c.1620G>A ENSP00000256578.3:p.Arg540=
ENST00000342115.8:c.1377G>A ENSP00000345498.4:p.Arg459=
ENST00000358729.8:c.1395G>A ENSP00000351573.4:p.Arg465=
ENST00000369840.6:c.1531G>A
ENST00000393688.7:c.1263G>A ENSP00000377292.3:p.Arg421=
ENST00000526301.5:n.1659G>A
ENST00000528454.5:c.1266G>A ENSP00000437164.1:p.Arg422=
ENST00000528667.5:c.1620G>A ENSP00000436541.1:p.Arg540=
ENST00000532851.1:n.168G>A
ENST00000533132.1:n.160G>A
NM_001257360.1:c.1620G>A NP_001244289.1:p.Arg540=
NM_001257361.1:c.1266G>A NP_001244290.1:p.Arg422=
NM_001308170.1:c.1395G>A NP_001295099.1:p.Arg465=
NM_004037.7:c.1620G>A NP_004028.3:p.Arg540=
NM_139156.3:c.1377G>A NP_631895.1:p.Arg459=
NM_203404.1:c.1263G>A NP_981949.1:p.Arg421=
XM_011541247.1:c.1833G>A XP_011539549.1:p.Arg611=
XM_011541248.1:c.1782+198G>A XP_011539550.1:n.1782+198G>A
XR_946607.1:n.1856G>A
XM_024446431.1:c.1395G>A XP_024302199.1:p.Arg465=
XM_024446432.1:c.1430+198G>A XP_024302200.1:n.1430+198G>A
XR_002956282.1:n.2031G>A
NM_001257360.2:c.1620G>A NP_001244289.1:p.Arg540=
NM_001368809.2:c.1458G>A MANE Select NP_001355738.1:p.Arg486=
NM_004037.9:c.1458G>A NP_004028.4:p.Arg486=
NM_001257361.2:c.1266G>A NP_001244290.1:p.Arg422=
NM_139156.4:c.1377G>A NP_631895.1:p.Arg459=