Canonical Allele Identifier: CA2346678780

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671641G= , CM000682.2:g.3671641G=	GRCh38
NC_000020.10:g.3652288G= , CM000682.1:g.3652288G=	GRCh37
NC_000020.9:g.3600288G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1845C= MANE Select	ENSP00000348912.3:p.Ala615=
ENST00000350009.6:c.1845C=	ENSP00000322550.5:p.Ala615=
ENST00000356518.6:c.1845C=	ENSP00000348912.2:p.Ala615=
ENST00000379861.8:c.1845C=	ENSP00000369190.4:p.Ala615=
ENST00000466620.5:n.1484C=
ENST00000617732.1:c.*632-184C=	ENSP00000483343.1:n.*632-184C=
ENST00000619289.4:c.1485C=	ENSP00000484600.1:p.Ala495=
NM_001282447.1:c.1845C=	NP_001269376.1:p.Ala615=
NM_025220.3:c.1845C=	NP_079496.1:p.Ala615=
NM_153202.2:c.1845C=	NP_694882.1:p.Ala615=
XM_005260843.1:c.1884C=	XP_005260900.1:p.Ala628=
XM_006723639.1:c.1884C=	XP_006723702.1:p.Ala628=
XM_006723640.1:c.1875C=	XP_006723703.1:p.Ala625=
XM_011529366.1:c.1881C=	XP_011527668.1:p.Ala627=
XM_011529367.1:c.1842C=	XP_011527669.1:p.Ala614=
XM_011529368.1:c.1884C=	XP_011527670.1:p.Ala628=
XM_011529369.1:c.1852C=	XP_011527671.1:p.Pro618=
XM_011529370.1:c.1852C=	XP_011527672.1:p.Pro618=
XM_011529373.1:c.882C=	XP_011527675.1:p.Ala294=
XR_937151.1:n.1988C=
XR_937152.1:n.1988C=
XR_937153.1:n.1869C=
XR_937154.1:n.1869C=
XR_937155.1:n.1790C=
XR_937157.1:n.1792C=
NM_001282447.2:c.1845C=	NP_001269376.1:p.Ala615=
NM_025220.4:c.1845C=	NP_079496.1:p.Ala615=
NM_153202.3:c.1845C=	NP_694882.1:p.Ala615=
XM_011529373.2:c.882C=	XP_011527675.1:p.Ala294=
XR_001754405.1:n.1956C=
XR_002958534.1:n.2065C=
NM_001282447.3:c.1845C=	NP_001269376.1:p.Ala615=
NM_025220.5:c.1845C= MANE Select	NP_079496.1:p.Ala615=
NM_153202.4:c.1845C=	NP_694882.1:p.Ala615=