Canonical Allele Identifier: CA1188179381
Gene: AMPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628653C= , CM000663.2:g.109628653C= GRCh38
NC_000001.10:g.110171275C= , CM000663.1:g.110171275C= GRCh37
NC_000001.9:g.109972798C= NCBI36
NG_034075.1:g.13841C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1418C= ENSP00000256578.4:p.Ser473=
ENST00000358729.9:c.1418C= ENSP00000351573.5:p.Ser473=
ENST00000369840.7:c.1418C= ENSP00000358855.3:p.Ser473=
ENST00000474459.6:n.2037C=
ENST00000476688.3:c.1100C= ENSP00000437025.2:p.Ser367=
ENST00000486282.7:n.2374C=
ENST00000524975.2:n.1899C=
ENST00000525415.2:n.1934C=
ENST00000526301.6:n.1481C=
ENST00000527846.7:n.1273C=
ENST00000528667.7:c.1418C= MANE Select ENSP00000436541.2:p.Ser473=
ENST00000531203.6:c.1226C= ENSP00000431975.2:p.Ser409=
ENST00000531734.6:c.1337C= ENSP00000433739.2:p.Ser446=
ENST00000652975.2:c.*1170C= ENSP00000499620.2:n.*1170C=
ENST00000654851.1:n.1260C=
ENST00000655992.1:c.1226C= ENSP00000499740.1:p.Ser409=
ENST00000659122.2:c.1407+158C= ENSP00000499621.2:n.1407+158C=
ENST00000663749.1:c.*1165C= ENSP00000499739.1:n.*1165C=
ENST00000667949.2:c.818C= ENSP00000499465.2:p.Ser273=
ENST00000668421.1:c.*1359C= ENSP00000499362.1:n.*1359C=
ENST00000679379.1:c.*1170C= ENSP00000505528.1:n.*1170C=
ENST00000679593.1:c.1418C= ENSP00000505999.1:p.Ser473=
ENST00000679880.1:n.1954C=
ENST00000679892.1:c.*1186C= ENSP00000504882.1:n.*1186C=
ENST00000679981.1:c.*1432C= ENSP00000506422.1:n.*1432C=
ENST00000680132.1:c.*1368C= ENSP00000505950.1:n.*1368C=
ENST00000680148.1:c.*1170C= ENSP00000505994.1:n.*1170C=
ENST00000680170.1:n.2283C=
ENST00000680192.1:n.2376C=
ENST00000680519.1:n.1654C=
ENST00000680531.1:c.*1165C= ENSP00000506332.1:n.*1165C=
ENST00000680820.1:c.*1170C= ENSP00000505735.1:n.*1170C=
ENST00000680832.1:c.*1518C= ENSP00000505774.1:n.*1518C=
ENST00000680929.1:c.*1107C= ENSP00000504916.1:n.*1107C=
ENST00000681108.1:c.*1245+158C= ENSP00000506701.1:n.*1245+158C=
ENST00000681121.1:c.*528C= ENSP00000506466.1:n.*528C=
ENST00000681132.1:c.*1184C= ENSP00000506195.1:n.*1184C=
ENST00000681181.1:c.*1403C= ENSP00000506038.1:n.*1403C=
ENST00000681218.1:c.*1691C= ENSP00000505976.1:n.*1691C=
ENST00000681246.1:c.*1074C= ENSP00000505534.1:n.*1074C=
ENST00000681496.1:c.*1691C= ENSP00000505948.1:n.*1691C=
ENST00000681834.1:n.1757C=
ENST00000681862.1:c.*1544C= ENSP00000505537.1:n.*1544C=
ENST00000256578.7:c.1580C= ENSP00000256578.3:p.Ser527=
ENST00000342115.8:c.1337C= ENSP00000345498.4:p.Ser446=
ENST00000358729.8:c.1355C= ENSP00000351573.4:p.Ser452=
ENST00000369840.6:c.1491C=
ENST00000393688.7:c.1223C= ENSP00000377292.3:p.Ser408=
ENST00000526301.5:n.1619C=
ENST00000528454.5:c.1226C= ENSP00000437164.1:p.Ser409=
ENST00000528667.5:c.1580C= ENSP00000436541.1:p.Ser527=
ENST00000532851.1:n.128C=
ENST00000533132.1:n.120C=
NM_001257360.1:c.1580C= NP_001244289.1:p.Ser527=
NM_001257361.1:c.1226C= NP_001244290.1:p.Ser409=
NM_001308170.1:c.1355C= NP_001295099.1:p.Ser452=
NM_004037.7:c.1580C= NP_004028.3:p.Ser527=
NM_139156.3:c.1337C= NP_631895.1:p.Ser446=
NM_203404.1:c.1223C= NP_981949.1:p.Ser408=
XM_011541247.1:c.1793C= XP_011539549.1:p.Ser598=
XM_011541248.1:c.1782+158C= XP_011539550.1:n.1782+158C=
XR_946607.1:n.1816C=
XM_024446431.1:c.1355C= XP_024302199.1:p.Ser452=
XM_024446432.1:c.1430+158C= XP_024302200.1:n.1430+158C=
XR_002956282.1:n.1991C=
NM_001257360.2:c.1580C= NP_001244289.1:p.Ser527=
NM_001368809.2:c.1418C= MANE Select NP_001355738.1:p.Ser473=
NM_004037.9:c.1418C= NP_004028.4:p.Ser473=
NM_001257361.2:c.1226C= NP_001244290.1:p.Ser409=
NM_139156.4:c.1337C= NP_631895.1:p.Ser446=