Canonical Allele Identifier: CA2346678842

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671751G= , CM000682.2:g.3671751G=	GRCh38
NC_000020.10:g.3652398G= , CM000682.1:g.3652398G=	GRCh37
NC_000020.9:g.3600398G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1735C= MANE Select	ENSP00000348912.3:p.Gln579=
ENST00000350009.6:c.1735C=	ENSP00000322550.5:p.Gln579=
ENST00000356518.6:c.1735C=	ENSP00000348912.2:p.Gln579=
ENST00000379861.8:c.1735C=	ENSP00000369190.4:p.Gln579=
ENST00000466620.5:n.1374C=
ENST00000617732.1:c.*632-294C=	ENSP00000483343.1:n.*632-294C=
ENST00000619289.4:c.1375C=	ENSP00000484600.1:p.Gln459=
NM_001282447.1:c.1735C=	NP_001269376.1:p.Gln579=
NM_025220.3:c.1735C=	NP_079496.1:p.Gln579=
NM_153202.2:c.1735C=	NP_694882.1:p.Gln579=
XM_005260843.1:c.1774C=	XP_005260900.1:p.Gln592=
XM_006723639.1:c.1774C=	XP_006723702.1:p.Gln592=
XM_006723640.1:c.1765C=	XP_006723703.1:p.Gln589=
XM_011529366.1:c.1771C=	XP_011527668.1:p.Gln591=
XM_011529367.1:c.1732C=	XP_011527669.1:p.Gln578=
XM_011529368.1:c.1774C=	XP_011527670.1:p.Gln592=
XM_011529369.1:c.1742C=	XP_011527671.1:p.Pro581=
XM_011529370.1:c.1742C=	XP_011527672.1:p.Pro581=
XM_011529373.1:c.772C=	XP_011527675.1:p.Gln258=
XR_937151.1:n.1878C=
XR_937152.1:n.1878C=
XR_937153.1:n.1759C=
XR_937154.1:n.1759C=
XR_937155.1:n.1680C=
XR_937157.1:n.1682C=
NM_001282447.2:c.1735C=	NP_001269376.1:p.Gln579=
NM_025220.4:c.1735C=	NP_079496.1:p.Gln579=
NM_153202.3:c.1735C=	NP_694882.1:p.Gln579=
XM_011529373.2:c.772C=	XP_011527675.1:p.Gln258=
XR_001754405.1:n.1846C=
XR_002958534.1:n.1955C=
NM_001282447.3:c.1735C=	NP_001269376.1:p.Gln579=
NM_025220.5:c.1735C= MANE Select	NP_079496.1:p.Gln579=
NM_153202.4:c.1735C=	NP_694882.1:p.Gln579=