Canonical Allele Identifier: CA2346678823

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671717A= , CM000682.2:g.3671717A=	GRCh38
NC_000020.10:g.3652364A= , CM000682.1:g.3652364A=	GRCh37
NC_000020.9:g.3600364A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1769T= MANE Select	ENSP00000348912.3:p.Met590=
ENST00000350009.6:c.1769T=	ENSP00000322550.5:p.Met590=
ENST00000356518.6:c.1769T=	ENSP00000348912.2:p.Met590=
ENST00000379861.8:c.1769T=	ENSP00000369190.4:p.Met590=
ENST00000466620.5:n.1408T=
ENST00000617732.1:c.*632-260T=	ENSP00000483343.1:n.*632-260T=
ENST00000619289.4:c.1409T=	ENSP00000484600.1:p.Met470=
NM_001282447.1:c.1769T=	NP_001269376.1:p.Met590=
NM_025220.3:c.1769T=	NP_079496.1:p.Met590=
NM_153202.2:c.1769T=	NP_694882.1:p.Met590=
XM_005260843.1:c.1808T=	XP_005260900.1:p.Met603=
XM_006723639.1:c.1808T=	XP_006723702.1:p.Met603=
XM_006723640.1:c.1799T=	XP_006723703.1:p.Met600=
XM_011529366.1:c.1805T=	XP_011527668.1:p.Met602=
XM_011529367.1:c.1766T=	XP_011527669.1:p.Met589=
XM_011529368.1:c.1808T=	XP_011527670.1:p.Met603=
XM_011529369.1:c.1776T=	XP_011527671.1:p.His592=
XM_011529370.1:c.1776T=	XP_011527672.1:p.His592=
XM_011529373.1:c.806T=	XP_011527675.1:p.Met269=
XR_937151.1:n.1912T=
XR_937152.1:n.1912T=
XR_937153.1:n.1793T=
XR_937154.1:n.1793T=
XR_937155.1:n.1714T=
XR_937157.1:n.1716T=
NM_001282447.2:c.1769T=	NP_001269376.1:p.Met590=
NM_025220.4:c.1769T=	NP_079496.1:p.Met590=
NM_153202.3:c.1769T=	NP_694882.1:p.Met590=
XM_011529373.2:c.806T=	XP_011527675.1:p.Met269=
XR_001754405.1:n.1880T=
XR_002958534.1:n.1989T=
NM_001282447.3:c.1769T=	NP_001269376.1:p.Met590=
NM_025220.5:c.1769T= MANE Select	NP_079496.1:p.Met590=
NM_153202.4:c.1769T=	NP_694882.1:p.Met590=