Canonical Allele Identifier: CA2346679085

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3672188A= , CM000682.2:g.3672188A=	GRCh38
NC_000020.10:g.3652835A= , CM000682.1:g.3652835A=	GRCh37
NC_000020.9:g.3600835A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_025220.5:c.1543T= MANE Select	NP_079496.1:p.Trp515=
ENST00000356518.7:c.1543T= MANE Select	ENSP00000348912.3:p.Trp515=
NM_001282447.1:c.1543T=	NP_001269376.1:p.Trp515=
NM_001282447.2:c.1543T=	NP_001269376.1:p.Trp515=
NM_001282447.3:c.1543T=	NP_001269376.1:p.Trp515=
NM_025220.3:c.1543T=	NP_079496.1:p.Trp515=
NM_025220.4:c.1543T=	NP_079496.1:p.Trp515=
NM_153202.2:c.1543T=	NP_694882.1:p.Trp515=
NM_153202.3:c.1543T=	NP_694882.1:p.Trp515=
NM_153202.4:c.1543T=	NP_694882.1:p.Trp515=
ENST00000350009.6:c.1543T=	ENSP00000322550.5:p.Trp515=
ENST00000356518.6:c.1543T=	ENSP00000348912.2:p.Trp515=
ENST00000379861.8:c.1543T=	ENSP00000369190.4:p.Trp515=
ENST00000466620.5:n.1182T=
ENST00000617732.1:c.*632-731T=	ENSP00000483343.1:n.*632-731T=
ENST00000619289.4:c.1183T=	ENSP00000484600.1:p.Trp395=
XM_005260843.1:c.1582T=	XP_005260900.1:p.Trp528=
XM_006723639.1:c.1582T=	XP_006723702.1:p.Trp528=
XM_006723640.1:c.1573T=	XP_006723703.1:p.Trp525=
XM_011529366.1:c.1579T=	XP_011527668.1:p.Trp527=
XM_011529367.1:c.1540T=	XP_011527669.1:p.Trp514=
XM_011529368.1:c.1582T=	XP_011527670.1:p.Trp528=
XM_011529369.1:c.1582T=	XP_011527671.1:p.Trp528=
XM_011529370.1:c.1582T=	XP_011527672.1:p.Trp528=
XM_011529373.1:c.580T=	XP_011527675.1:p.Trp194=
XM_011529373.2:c.580T=	XP_011527675.1:p.Trp194=
XR_001754405.1:n.1686T=
XR_002958534.1:n.1763T=
XR_937151.1:n.1686T=
XR_937152.1:n.1686T=
XR_937153.1:n.1622-203T=
XR_937154.1:n.1622-203T=
XR_937155.1:n.1543-203T=
XR_937157.1:n.1545-203T=