Canonical Allele Identifier: CA992822

Gene: AMPD2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109626439G>A , CM000663.2:g.109626439G>A	GRCh38
NC_000001.10:g.110169061G>A , CM000663.1:g.110169061G>A	GRCh37
NC_000001.9:g.109970584G>A	NCBI36
NG_034075.1:g.11627G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256578.8:c.531+12G>A	ENSP00000256578.4:n.531+12G>A
ENST00000358729.9:c.531+12G>A	ENSP00000351573.5:n.531+12G>A
ENST00000369840.7:c.531+12G>A	ENSP00000358855.3:n.531+12G>A
ENST00000474459.6:n.888+12G>A
ENST00000476688.3:c.213+12G>A	ENSP00000437025.2:n.213+12G>A
ENST00000486282.7:n.594G>A
ENST00000524975.2:n.491+12G>A
ENST00000525415.2:n.789+12G>A
ENST00000526301.6:n.594+12G>A
ENST00000527846.7:n.386+12G>A
ENST00000528667.7:c.531+12G>A MANE Select	ENSP00000436541.2:n.531+12G>A
ENST00000531203.6:c.339+12G>A	ENSP00000431975.2:n.339+12G>A
ENST00000531734.6:c.450+12G>A	ENSP00000433739.2:n.450+12G>A
ENST00000652975.2:c.*283+12G>A	ENSP00000499620.2:n.*283+12G>A
ENST00000654851.1:n.373+12G>A
ENST00000655992.1:c.339+12G>A	ENSP00000499740.1:n.339+12G>A
ENST00000659122.2:c.531+12G>A	ENSP00000499621.2:n.531+12G>A
ENST00000663749.1:c.*283+12G>A	ENSP00000499739.1:n.*283+12G>A
ENST00000667949.2:c.-70+12G>A	ENSP00000499465.2:n.-70+12G>A
ENST00000668421.1:c.*472+12G>A	ENSP00000499362.1:n.*472+12G>A
ENST00000679379.1:c.*283+12G>A	ENSP00000505528.1:n.*283+12G>A
ENST00000679593.1:c.531+12G>A	ENSP00000505999.1:n.531+12G>A
ENST00000679880.1:n.789+12G>A
ENST00000679892.1:c.*283+12G>A	ENSP00000504882.1:n.*283+12G>A
ENST00000679981.1:c.*283+12G>A	ENSP00000506422.1:n.*283+12G>A
ENST00000680132.1:c.*283+12G>A	ENSP00000505950.1:n.*283+12G>A
ENST00000680148.1:c.*283+12G>A	ENSP00000505994.1:n.*283+12G>A
ENST00000680170.1:n.789+12G>A
ENST00000680192.1:n.882+12G>A
ENST00000680519.1:n.751+12G>A
ENST00000680531.1:c.*283+12G>A	ENSP00000506332.1:n.*283+12G>A
ENST00000680820.1:c.*283+12G>A	ENSP00000505735.1:n.*283+12G>A
ENST00000680832.1:c.*283+12G>A	ENSP00000505774.1:n.*283+12G>A
ENST00000680929.1:c.*283+12G>A	ENSP00000504916.1:n.*283+12G>A
ENST00000681108.1:c.*283+12G>A	ENSP00000506701.1:n.*283+12G>A
ENST00000681121.1:c.339+12G>A	ENSP00000506466.1:n.339+12G>A
ENST00000681132.1:c.*283+12G>A	ENSP00000506195.1:n.*283+12G>A
ENST00000681181.1:c.*283+12G>A	ENSP00000506038.1:n.*283+12G>A
ENST00000681218.1:c.*283+12G>A	ENSP00000505976.1:n.*283+12G>A
ENST00000681246.1:c.*187+12G>A	ENSP00000505534.1:n.*187+12G>A
ENST00000681496.1:c.*283+12G>A	ENSP00000505948.1:n.*283+12G>A
ENST00000681834.1:n.608+12G>A
ENST00000681862.1:c.*283+12G>A	ENSP00000505537.1:n.*283+12G>A
ENST00000256578.7:c.693+12G>A	ENSP00000256578.3:n.693+12G>A
ENST00000342115.8:c.450+12G>A	ENSP00000345498.4:n.450+12G>A
ENST00000358729.8:c.468+12G>A	ENSP00000351573.4:n.468+12G>A
ENST00000369840.6:c.604+12G>A
ENST00000393688.7:c.336+12G>A	ENSP00000377292.3:n.336+12G>A
ENST00000474459.5:c.-70+12G>A	ENSP00000432344.1:n.-70+12G>A
ENST00000486282.6:n.563G>A
ENST00000525415.1:n.140+12G>A
ENST00000526301.5:n.732+12G>A
ENST00000528454.5:c.339+12G>A	ENSP00000437164.1:n.339+12G>A
ENST00000528667.5:c.693+12G>A	ENSP00000436541.1:n.693+12G>A
ENST00000534144.1:n.357+12G>A
NM_001257360.1:c.693+12G>A	NP_001244289.1:n.693+12G>A
NM_001257361.1:c.339+12G>A	NP_001244290.1:n.339+12G>A
NM_001308170.1:c.468+12G>A	NP_001295099.1:n.468+12G>A
NM_004037.7:c.693+12G>A	NP_004028.3:n.693+12G>A
NM_139156.3:c.450+12G>A	NP_631895.1:n.450+12G>A
NM_203404.1:c.336+12G>A	NP_981949.1:n.336+12G>A
XM_011541247.1:c.906+12G>A	XP_011539549.1:n.906+12G>A
XM_011541248.1:c.906+12G>A	XP_011539550.1:n.906+12G>A
XR_946607.1:n.929+12G>A
XM_024446431.1:c.468+12G>A	XP_024302199.1:n.468+12G>A
XM_024446432.1:c.468+12G>A	XP_024302200.1:n.468+12G>A
XR_002956282.1:n.1104+12G>A
NM_001257360.2:c.693+12G>A	NP_001244289.1:n.693+12G>A
NM_001368809.2:c.531+12G>A MANE Select	NP_001355738.1:n.531+12G>A
NM_004037.9:c.531+12G>A	NP_004028.4:n.531+12G>A
NM_001257361.2:c.339+12G>A	NP_001244290.1:n.339+12G>A
NM_139156.4:c.450+12G>A	NP_631895.1:n.450+12G>A