Canonical Allele Identifier: CA4330273

Gene: ADAM22

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.88125640C>G , CM000669.2:g.88125640C>G	GRCh38
NC_000007.13:g.87754955C>G , CM000669.1:g.87754955C>G	GRCh37
NC_000007.12:g.87592891C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000398203.8:c.560C>G	ENSP00000381261.4:p.Pro187Arg
ENST00000413139.2:c.659C>G MANE Select	ENSP00000412085.2:p.Pro220Arg
ENST00000682337.1:c.332C>G	ENSP00000507249.1:p.Pro111Arg
ENST00000683525.1:c.659C>G	ENSP00000506730.1:p.Pro220Arg
ENST00000684002.1:c.659C>G	ENSP00000508320.1:p.Pro220Arg
ENST00000265727.11:c.659C>G	ENSP00000265727.7:p.Pro220Arg
ENST00000398201.8:c.659C>G	ENSP00000381260.4:p.Pro220Arg
ENST00000398203.7:c.560C>G	ENSP00000381261.3:p.Pro187Arg
ENST00000398204.8:c.659C>G	ENSP00000381262.4:p.Pro220Arg
ENST00000398209.7:c.659C>G	ENSP00000381267.3:p.Pro220Arg
ENST00000439864.5:c.659C>G	ENSP00000391334.1:p.Pro220Arg
ENST00000478920.1:n.365C>G
NM_004194.3:c.659C>G	NP_004185.1:p.Pro220Arg
NM_016351.4:c.659C>G	NP_057435.2:p.Pro220Arg
NM_021721.3:c.659C>G	NP_068367.1:p.Pro220Arg
NM_021722.4:c.659C>G	NP_068368.2:p.Pro220Arg
NM_021723.3:c.659C>G	NP_068369.1:p.Pro220Arg
XM_005250445.2:c.815C>G	XP_005250502.1:p.Pro272Arg
XM_006716028.2:c.815C>G	XP_006716091.1:p.Pro272Arg
XM_006716029.2:c.815C>G	XP_006716092.1:p.Pro272Arg
XM_011516318.1:c.659C>G	XP_011514620.1:p.Pro220Arg
XM_011516319.1:c.656C>G	XP_011514621.1:p.Pro219Arg
XM_011516320.1:c.815C>G	XP_011514622.1:p.Pro272Arg
XM_011516321.1:c.815C>G	XP_011514623.1:p.Pro272Arg
XM_011516322.1:c.659C>G	XP_011514624.1:p.Pro220Arg
XM_011516323.1:c.659C>G	XP_011514625.1:p.Pro220Arg
XM_011516324.1:c.437C>G	XP_011514626.1:p.Pro146Arg
NM_001324417.1:c.656C>G	NP_001311346.1:p.Pro219Arg
NM_001324418.1:c.659C>G	NP_001311347.1:p.Pro220Arg
NM_001324419.1:c.656C>G	NP_001311348.1:p.Pro219Arg
NM_001324420.1:c.659C>G	NP_001311349.1:p.Pro220Arg
NM_001324421.1:c.659C>G	NP_001311350.1:p.Pro220Arg
NM_004194.4:c.659C>G	NP_004185.1:p.Pro220Arg
NM_016351.5:c.659C>G	NP_057435.2:p.Pro220Arg
NM_021721.4:c.659C>G	NP_068367.1:p.Pro220Arg
NM_021722.5:c.659C>G	NP_068368.2:p.Pro220Arg
NM_021723.4:c.659C>G	NP_068369.1:p.Pro220Arg
XM_005250445.4:c.815C>G	XP_005250502.1:p.Pro272Arg
XM_006716028.4:c.815C>G	XP_006716091.1:p.Pro272Arg
XM_006716029.4:c.815C>G	XP_006716092.1:p.Pro272Arg
XM_011516318.2:c.659C>G	XP_011514620.1:p.Pro220Arg
XM_011516319.3:c.656C>G	XP_011514621.1:p.Pro219Arg
XM_011516320.3:c.815C>G	XP_011514622.1:p.Pro272Arg
XM_011516321.3:c.815C>G	XP_011514623.1:p.Pro272Arg
XM_011516322.2:c.659C>G	XP_011514624.1:p.Pro220Arg
XM_011516323.2:c.659C>G	XP_011514625.1:p.Pro220Arg
XM_011516324.2:c.437C>G	XP_011514626.1:p.Pro146Arg
XM_017012329.2:c.710C>G	XP_016867818.1:p.Pro237Arg
XM_017012330.2:c.710C>G	XP_016867819.1:p.Pro237Arg
XM_017012331.2:c.656C>G	XP_016867820.1:p.Pro219Arg
XM_017012332.2:c.659C>G	XP_016867821.1:p.Pro220Arg
XM_017012333.2:c.659C>G	XP_016867822.1:p.Pro220Arg
XM_017012334.2:c.710C>G	XP_016867823.1:p.Pro237Arg
XM_017012335.2:c.710C>G	XP_016867824.1:p.Pro237Arg
XM_017012336.2:c.659C>G	XP_016867825.1:p.Pro220Arg
XM_017012337.2:c.710C>G	XP_016867826.1:p.Pro237Arg
XM_017012338.2:c.656C>G	XP_016867827.1:p.Pro219Arg
XM_017012339.2:c.710C>G	XP_016867828.1:p.Pro237Arg
XM_017012341.2:c.-468C>G	XP_016867830.1:n.-468C>G
NM_001324417.2:c.656C>G	NP_001311346.1:p.Pro219Arg
NM_001324418.2:c.659C>G MANE Select	NP_001311347.1:p.Pro220Arg
NM_001324419.2:c.656C>G	NP_001311348.1:p.Pro219Arg
NM_001324420.2:c.659C>G	NP_001311349.1:p.Pro220Arg
NM_001324421.2:c.659C>G	NP_001311350.1:p.Pro220Arg
NM_016351.6:c.659C>G	NP_057435.2:p.Pro220Arg
NM_021722.6:c.659C>G	NP_068368.2:p.Pro220Arg
NM_021723.5:c.659C>G	NP_068369.1:p.Pro220Arg
NM_001391975.1:c.710C>G	NP_001378904.1:p.Pro237Arg
NM_001391976.1:c.659C>G	NP_001378905.1:p.Pro220Arg
NM_001391977.1:c.659C>G	NP_001378906.1:p.Pro220Arg
NM_001391978.1:c.656C>G	NP_001378907.1:p.Pro219Arg
NM_001391979.1:c.656C>G	NP_001378908.1:p.Pro219Arg
NM_001391980.1:c.710C>G	NP_001378909.1:p.Pro237Arg
NM_001391981.1:c.656C>G	NP_001378910.1:p.Pro219Arg
NM_001391982.1:c.710C>G	NP_001378911.1:p.Pro237Arg
NM_004194.5:c.659C>G	NP_004185.1:p.Pro220Arg
NM_021721.5:c.659C>G	NP_068367.1:p.Pro220Arg