Canonical Allele Identifier: CA4330022

Gene: ADAM22

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.87934559G>A , CM000669.2:g.87934559G>A	GRCh38
NC_000007.13:g.87563874G>A , CM000669.1:g.87563874G>A	GRCh37
NC_000007.12:g.87401810G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413139.2:c.85+9G>A MANE Select	ENSP00000412085.2:n.85+9G>A
ENST00000683525.1:c.85+9G>A	ENSP00000506730.1:n.85+9G>A
ENST00000684002.1:c.85+9G>A	ENSP00000508320.1:n.85+9G>A
ENST00000265727.11:c.85+9G>A	ENSP00000265727.7:n.85+9G>A
ENST00000398201.8:c.85+9G>A	ENSP00000381260.4:n.85+9G>A
ENST00000398204.8:c.85+9G>A	ENSP00000381262.4:n.85+9G>A
ENST00000398209.7:c.85+9G>A	ENSP00000381267.3:n.85+9G>A
ENST00000412441.5:c.85+9G>A	ENSP00000413899.1:n.85+9G>A
ENST00000439864.5:c.85+9G>A	ENSP00000391334.1:n.85+9G>A
NM_004194.3:c.85+9G>A	NP_004185.1:n.85+9G>A
NM_016351.4:c.85+9G>A	NP_057435.2:n.85+9G>A
NM_021721.3:c.85+9G>A	NP_068367.1:n.85+9G>A
NM_021722.4:c.85+9G>A	NP_068368.2:n.85+9G>A
NM_021723.3:c.85+9G>A	NP_068369.1:n.85+9G>A
XM_011516318.1:c.85+9G>A	XP_011514620.1:n.85+9G>A
XM_011516319.1:c.85+9G>A	XP_011514621.1:n.85+9G>A
XM_011516322.1:c.85+9G>A	XP_011514624.1:n.85+9G>A
XM_011516323.1:c.85+9G>A	XP_011514625.1:n.85+9G>A
NM_001324417.1:c.85+9G>A	NP_001311346.1:n.85+9G>A
NM_001324418.1:c.85+9G>A	NP_001311347.1:n.85+9G>A
NM_001324419.1:c.85+9G>A	NP_001311348.1:n.85+9G>A
NM_001324420.1:c.85+9G>A	NP_001311349.1:n.85+9G>A
NM_001324421.1:c.85+9G>A	NP_001311350.1:n.85+9G>A
NM_004194.4:c.85+9G>A	NP_004185.1:n.85+9G>A
NM_016351.5:c.85+9G>A	NP_057435.2:n.85+9G>A
NM_021721.4:c.85+9G>A	NP_068367.1:n.85+9G>A
NM_021722.5:c.85+9G>A	NP_068368.2:n.85+9G>A
NM_021723.4:c.85+9G>A	NP_068369.1:n.85+9G>A
XM_011516318.2:c.85+9G>A	XP_011514620.1:n.85+9G>A
XM_011516319.3:c.85+9G>A	XP_011514621.1:n.85+9G>A
XM_011516322.2:c.85+9G>A	XP_011514624.1:n.85+9G>A
XM_011516323.2:c.85+9G>A	XP_011514625.1:n.85+9G>A
XM_017012329.2:c.85+9G>A	XP_016867818.1:n.85+9G>A
XM_017012330.2:c.85+9G>A	XP_016867819.1:n.85+9G>A
XM_017012331.2:c.85+9G>A	XP_016867820.1:n.85+9G>A
XM_017012332.2:c.85+9G>A	XP_016867821.1:n.85+9G>A
XM_017012333.2:c.85+9G>A	XP_016867822.1:n.85+9G>A
XM_017012334.2:c.85+9G>A	XP_016867823.1:n.85+9G>A
XM_017012335.2:c.85+9G>A	XP_016867824.1:n.85+9G>A
XM_017012336.2:c.85+9G>A	XP_016867825.1:n.85+9G>A
XM_017012337.2:c.85+9G>A	XP_016867826.1:n.85+9G>A
XM_017012338.2:c.85+9G>A	XP_016867827.1:n.85+9G>A
XM_017012339.2:c.85+9G>A	XP_016867828.1:n.85+9G>A
XM_017012341.2:c.-1042+9G>A	XP_016867830.1:n.-1042+9G>A
NM_001324417.2:c.85+9G>A	NP_001311346.1:n.85+9G>A
NM_001324418.2:c.85+9G>A MANE Select	NP_001311347.1:n.85+9G>A
NM_001324419.2:c.85+9G>A	NP_001311348.1:n.85+9G>A
NM_001324420.2:c.85+9G>A	NP_001311349.1:n.85+9G>A
NM_001324421.2:c.85+9G>A	NP_001311350.1:n.85+9G>A
NM_016351.6:c.85+9G>A	NP_057435.2:n.85+9G>A
NM_021722.6:c.85+9G>A	NP_068368.2:n.85+9G>A
NM_021723.5:c.85+9G>A	NP_068369.1:n.85+9G>A
NM_001391975.1:c.85+9G>A	NP_001378904.1:n.85+9G>A
NM_001391976.1:c.85+9G>A	NP_001378905.1:n.85+9G>A
NM_001391977.1:c.85+9G>A	NP_001378906.1:n.85+9G>A
NM_001391978.1:c.85+9G>A	NP_001378907.1:n.85+9G>A
NM_001391979.1:c.85+9G>A	NP_001378908.1:n.85+9G>A
NM_001391980.1:c.85+9G>A	NP_001378909.1:n.85+9G>A
NM_001391981.1:c.85+9G>A	NP_001378910.1:n.85+9G>A
NM_001391982.1:c.85+9G>A	NP_001378911.1:n.85+9G>A
NM_004194.5:c.85+9G>A	NP_004185.1:n.85+9G>A
NM_021721.5:c.85+9G>A	NP_068367.1:n.85+9G>A