Canonical Allele Identifier: CA992942

Gene: AMPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109627353G>A , CM000663.2:g.109627353G>A	GRCh38
NC_000001.10:g.110169975G>A , CM000663.1:g.110169975G>A	GRCh37
NC_000001.9:g.109971498G>A	NCBI36
NG_034075.1:g.12541G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256578.8:c.860+37G>A	ENSP00000256578.4:n.860+37G>A
ENST00000358729.9:c.860+37G>A	ENSP00000351573.5:n.860+37G>A
ENST00000369840.7:c.860+37G>A	ENSP00000358855.3:n.860+37G>A
ENST00000474459.6:n.1479+37G>A
ENST00000476688.3:c.542+37G>A	ENSP00000437025.2:n.542+37G>A
ENST00000486282.7:n.1508G>A
ENST00000524975.2:n.1119G>A
ENST00000525415.2:n.1380+37G>A
ENST00000526301.6:n.923+37G>A
ENST00000527846.7:n.715+37G>A
ENST00000528667.7:c.860+37G>A MANE Select	ENSP00000436541.2:n.860+37G>A
ENST00000531203.6:c.668+37G>A	ENSP00000431975.2:n.668+37G>A
ENST00000531734.6:c.779+37G>A	ENSP00000433739.2:n.779+37G>A
ENST00000652975.2:c.*612+37G>A	ENSP00000499620.2:n.*612+37G>A
ENST00000654851.1:n.702+37G>A
ENST00000655992.1:c.668+37G>A	ENSP00000499740.1:n.668+37G>A
ENST00000659122.2:c.860+37G>A	ENSP00000499621.2:n.860+37G>A
ENST00000663749.1:c.*612+37G>A	ENSP00000499739.1:n.*612+37G>A
ENST00000667949.2:c.260+37G>A	ENSP00000499465.2:n.260+37G>A
ENST00000668421.1:c.*801+37G>A	ENSP00000499362.1:n.*801+37G>A
ENST00000679379.1:c.*612+37G>A	ENSP00000505528.1:n.*612+37G>A
ENST00000679593.1:c.860+37G>A	ENSP00000505999.1:n.860+37G>A
ENST00000679880.1:n.1380+37G>A
ENST00000679892.1:c.*612+37G>A	ENSP00000504882.1:n.*612+37G>A
ENST00000679981.1:c.*874+37G>A	ENSP00000506422.1:n.*874+37G>A
ENST00000680132.1:c.*649G>A	ENSP00000505950.1:n.*649G>A
ENST00000680148.1:c.*612+37G>A	ENSP00000505994.1:n.*612+37G>A
ENST00000680170.1:n.1417G>A
ENST00000680192.1:n.1510G>A
ENST00000680519.1:n.1080+37G>A
ENST00000680531.1:c.*612+37G>A	ENSP00000506332.1:n.*612+37G>A
ENST00000680820.1:c.*612+37G>A	ENSP00000505735.1:n.*612+37G>A
ENST00000680832.1:c.*874+37G>A	ENSP00000505774.1:n.*874+37G>A
ENST00000680929.1:c.*612+37G>A	ENSP00000504916.1:n.*612+37G>A
ENST00000681108.1:c.*612+37G>A	ENSP00000506701.1:n.*612+37G>A
ENST00000681121.1:c.668+37G>A	ENSP00000506466.1:n.668+37G>A
ENST00000681132.1:c.*626+23G>A	ENSP00000506195.1:n.*626+23G>A
ENST00000681181.1:c.*612+37G>A	ENSP00000506038.1:n.*612+37G>A
ENST00000681218.1:c.*911G>A	ENSP00000505976.1:n.*911G>A
ENST00000681246.1:c.*516+37G>A	ENSP00000505534.1:n.*516+37G>A
ENST00000681496.1:c.*911G>A	ENSP00000505948.1:n.*911G>A
ENST00000681834.1:n.1199+37G>A
ENST00000681862.1:c.*911G>A	ENSP00000505537.1:n.*911G>A
ENST00000256578.7:c.1022+37G>A	ENSP00000256578.3:n.1022+37G>A
ENST00000342115.8:c.779+37G>A	ENSP00000345498.4:n.779+37G>A
ENST00000358729.8:c.797+37G>A	ENSP00000351573.4:n.797+37G>A
ENST00000369840.6:c.933+37G>A
ENST00000393688.7:c.665+37G>A	ENSP00000377292.3:n.665+37G>A
ENST00000524975.1:n.431G>A
ENST00000526301.5:n.1061+37G>A
ENST00000528454.5:c.668+37G>A	ENSP00000437164.1:n.668+37G>A
ENST00000528667.5:c.1022+37G>A	ENSP00000436541.1:n.1022+37G>A
NM_001257360.1:c.1022+37G>A	NP_001244289.1:n.1022+37G>A
NM_001257361.1:c.668+37G>A	NP_001244290.1:n.668+37G>A
NM_001308170.1:c.797+37G>A	NP_001295099.1:n.797+37G>A
NM_004037.7:c.1022+37G>A	NP_004028.3:n.1022+37G>A
NM_139156.3:c.779+37G>A	NP_631895.1:n.779+37G>A
NM_203404.1:c.665+37G>A	NP_981949.1:n.665+37G>A
XM_011541247.1:c.1235+37G>A	XP_011539549.1:n.1235+37G>A
XM_011541248.1:c.1235+37G>A	XP_011539550.1:n.1235+37G>A
XR_946607.1:n.1258+37G>A
XM_024446431.1:c.797+37G>A	XP_024302199.1:n.797+37G>A
XM_024446432.1:c.797+37G>A	XP_024302200.1:n.797+37G>A
XR_002956282.1:n.1433+37G>A
NM_001257360.2:c.1022+37G>A	NP_001244289.1:n.1022+37G>A
NM_001368809.2:c.860+37G>A MANE Select	NP_001355738.1:n.860+37G>A
NM_004037.9:c.860+37G>A	NP_004028.4:n.860+37G>A
NM_001257361.2:c.668+37G>A	NP_001244290.1:n.668+37G>A
NM_139156.4:c.779+37G>A	NP_631895.1:n.779+37G>A