Canonical Allele Identifier: CA2346678691

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671492C= , CM000682.2:g.3671492C=	GRCh38
NC_000020.10:g.3652139C= , CM000682.1:g.3652139C=	GRCh37
NC_000020.9:g.3600139C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1910G= MANE Select	ENSP00000348912.3:p.Cys637=
ENST00000350009.6:c.1905+89G=	ENSP00000322550.5:n.1905+89G=
ENST00000356518.6:c.1910G=	ENSP00000348912.2:p.Cys637=
ENST00000379861.8:c.1910G=	ENSP00000369190.4:p.Cys637=
ENST00000466620.5:n.1544+89G=
ENST00000617732.1:c.*632-35G=	ENSP00000483343.1:n.*632-35G=
ENST00000619289.4:c.1550G=	ENSP00000484600.1:p.Cys517=
NM_001282447.1:c.1910G=	NP_001269376.1:p.Cys637=
NM_025220.3:c.1910G=	NP_079496.1:p.Cys637=
NM_153202.2:c.1905+89G=	NP_694882.1:n.1905+89G=
XM_005260843.1:c.1949G=	XP_005260900.1:p.Cys650=
XM_006723639.1:c.1949G=	XP_006723702.1:p.Cys650=
XM_006723640.1:c.1940G=	XP_006723703.1:p.Cys647=
XM_011529366.1:c.1946G=	XP_011527668.1:p.Cys649=
XM_011529367.1:c.1907G=	XP_011527669.1:p.Cys636=
XM_011529368.1:c.1944+89G=	XP_011527670.1:n.1944+89G=
XM_011529369.1:c.*9G=	XP_011527671.1:n.*9G=
XM_011529370.1:c.*4+89G=	XP_011527672.1:n.*4+89G=
XM_011529373.1:c.947G=	XP_011527675.1:p.Cys316=
XR_937151.1:n.2053G=
XR_937152.1:n.2053G=
XR_937153.1:n.1934G=
XR_937154.1:n.1934G=
XR_937155.1:n.1855G=
XR_937157.1:n.1857G=
NM_001282447.2:c.1910G=	NP_001269376.1:p.Cys637=
NM_025220.4:c.1910G=	NP_079496.1:p.Cys637=
NM_153202.3:c.1905+89G=	NP_694882.1:n.1905+89G=
XM_011529373.2:c.947G=	XP_011527675.1:p.Cys316=
XR_001754405.1:n.2021G=
XR_002958534.1:n.2130G=
NM_001282447.3:c.1910G=	NP_001269376.1:p.Cys637=
NM_025220.5:c.1910G= MANE Select	NP_079496.1:p.Cys637=
NM_153202.4:c.1905+89G=	NP_694882.1:n.1905+89G=