Canonical Allele Identifier: CA1188179409
Gene: AMPD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.109628748G= , CM000663.2:g.109628748G= GRCh38
NC_000001.10:g.110171370G= , CM000663.1:g.110171370G= GRCh37
NC_000001.9:g.109972893G= NCBI36
NG_034075.1:g.13936G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000256578.8:c.1513G= ENSP00000256578.4:p.Val505=
ENST00000358729.9:c.1513G= ENSP00000351573.5:p.Val505=
ENST00000369840.7:c.1513G= ENSP00000358855.3:p.Val505=
ENST00000474459.6:n.2132G=
ENST00000476688.3:c.1195G= ENSP00000437025.2:p.Val399=
ENST00000486282.7:n.2469G=
ENST00000524975.2:n.1994G=
ENST00000525415.2:n.2029G=
ENST00000526301.6:n.1576G=
ENST00000527846.7:n.1368G=
ENST00000528667.7:c.1513G= MANE Select ENSP00000436541.2:p.Val505=
ENST00000531203.6:c.1321G= ENSP00000431975.2:p.Val441=
ENST00000531734.6:c.1432G= ENSP00000433739.2:p.Val478=
ENST00000652975.2:c.*1265G= ENSP00000499620.2:n.*1265G=
ENST00000654851.1:n.1355G=
ENST00000655992.1:c.1321G= ENSP00000499740.1:p.Val441=
ENST00000659122.2:c.1407+253G= ENSP00000499621.2:n.1407+253G=
ENST00000663749.1:c.*1260G= ENSP00000499739.1:n.*1260G=
ENST00000667949.2:c.913G= ENSP00000499465.2:p.Val305=
ENST00000668421.1:c.*1454G= ENSP00000499362.1:n.*1454G=
ENST00000679379.1:c.*1265G= ENSP00000505528.1:n.*1265G=
ENST00000679593.1:c.1513G= ENSP00000505999.1:p.Val505=
ENST00000679880.1:n.2049G=
ENST00000679892.1:c.*1281G= ENSP00000504882.1:n.*1281G=
ENST00000679981.1:c.*1527G= ENSP00000506422.1:n.*1527G=
ENST00000680132.1:c.*1463G= ENSP00000505950.1:n.*1463G=
ENST00000680148.1:c.*1265G= ENSP00000505994.1:n.*1265G=
ENST00000680170.1:n.2378G=
ENST00000680192.1:n.2471G=
ENST00000680519.1:n.1749G=
ENST00000680531.1:c.*1260G= ENSP00000506332.1:n.*1260G=
ENST00000680820.1:c.*1265G= ENSP00000505735.1:n.*1265G=
ENST00000680832.1:c.*1613G= ENSP00000505774.1:n.*1613G=
ENST00000680929.1:c.*1202G= ENSP00000504916.1:n.*1202G=
ENST00000681108.1:c.*1245+253G= ENSP00000506701.1:n.*1245+253G=
ENST00000681121.1:c.*623G= ENSP00000506466.1:n.*623G=
ENST00000681132.1:c.*1279G= ENSP00000506195.1:n.*1279G=
ENST00000681181.1:c.*1498G= ENSP00000506038.1:n.*1498G=
ENST00000681218.1:c.*1786G= ENSP00000505976.1:n.*1786G=
ENST00000681246.1:c.*1169G= ENSP00000505534.1:n.*1169G=
ENST00000681496.1:c.*1786G= ENSP00000505948.1:n.*1786G=
ENST00000681834.1:n.1852G=
ENST00000681862.1:c.*1639G= ENSP00000505537.1:n.*1639G=
ENST00000256578.7:c.1675G= ENSP00000256578.3:p.Val559=
ENST00000342115.8:c.1432G= ENSP00000345498.4:p.Val478=
ENST00000358729.8:c.1450G= ENSP00000351573.4:p.Val484=
ENST00000369840.6:c.1586G=
ENST00000393688.7:c.1318G= ENSP00000377292.3:p.Val440=
ENST00000467071.1:n.35G=
ENST00000526301.5:n.1714G=
ENST00000528454.5:c.1321G= ENSP00000437164.1:p.Val441=
ENST00000528667.5:c.1675G= ENSP00000436541.1:p.Val559=
ENST00000532851.1:n.223G=
ENST00000533132.1:n.215G=
NM_001257360.1:c.1675G= NP_001244289.1:p.Val559=
NM_001257361.1:c.1321G= NP_001244290.1:p.Val441=
NM_001308170.1:c.1450G= NP_001295099.1:p.Val484=
NM_004037.7:c.1675G= NP_004028.3:p.Val559=
NM_139156.3:c.1432G= NP_631895.1:p.Val478=
NM_203404.1:c.1318G= NP_981949.1:p.Val440=
XM_011541247.1:c.1888G= XP_011539549.1:p.Val630=
XM_011541248.1:c.1782+253G= XP_011539550.1:n.1782+253G=
XR_946607.1:n.1911G=
XM_024446431.1:c.1450G= XP_024302199.1:p.Val484=
XM_024446432.1:c.1430+253G= XP_024302200.1:n.1430+253G=
XR_002956282.1:n.2086G=
NM_001257360.2:c.1675G= NP_001244289.1:p.Val559=
NM_001368809.2:c.1513G= MANE Select NP_001355738.1:p.Val505=
NM_004037.9:c.1513G= NP_004028.4:p.Val505=
NM_001257361.2:c.1321G= NP_001244290.1:p.Val441=
NM_139156.4:c.1432G= NP_631895.1:p.Val478=