Canonical Allele Identifier: CA2346678904

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671865T= , CM000682.2:g.3671865T=	GRCh38
NC_000020.10:g.3652512T= , CM000682.1:g.3652512T=	GRCh37
NC_000020.9:g.3600512T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1706+12A= MANE Select	ENSP00000348912.3:n.1706+12A=
ENST00000350009.6:c.1706+12A=	ENSP00000322550.5:n.1706+12A=
ENST00000356518.6:c.1706+12A=	ENSP00000348912.2:n.1706+12A=
ENST00000379861.8:c.1706+12A=	ENSP00000369190.4:n.1706+12A=
ENST00000466620.5:n.1345+12A=
ENST00000617732.1:c.*632-408A=	ENSP00000483343.1:n.*632-408A=
ENST00000619289.4:c.1346+12A=	ENSP00000484600.1:n.1346+12A=
NM_001282447.1:c.1706+12A=	NP_001269376.1:n.1706+12A=
NM_025220.3:c.1706+12A=	NP_079496.1:n.1706+12A=
NM_153202.2:c.1706+12A=	NP_694882.1:n.1706+12A=
XM_005260843.1:c.1745+12A=	XP_005260900.1:n.1745+12A=
XM_006723639.1:c.1745+12A=	XP_006723702.1:n.1745+12A=
XM_006723640.1:c.1736+12A=	XP_006723703.1:n.1736+12A=
XM_011529366.1:c.1742+12A=	XP_011527668.1:n.1742+12A=
XM_011529367.1:c.1703+12A=	XP_011527669.1:n.1703+12A=
XM_011529368.1:c.1745+12A=	XP_011527670.1:n.1745+12A=
XM_011529369.1:c.1713+12A=	XP_011527671.1:n.1713+12A=
XM_011529370.1:c.1713+12A=	XP_011527672.1:n.1713+12A=
XM_011529373.1:c.743+12A=	XP_011527675.1:n.743+12A=
XR_937151.1:n.1849+12A=
XR_937152.1:n.1849+12A=
XR_937153.1:n.1730+12A=
XR_937154.1:n.1730+12A=
XR_937155.1:n.1651+12A=
XR_937157.1:n.1653+12A=
NM_001282447.2:c.1706+12A=	NP_001269376.1:n.1706+12A=
NM_025220.4:c.1706+12A=	NP_079496.1:n.1706+12A=
NM_153202.3:c.1706+12A=	NP_694882.1:n.1706+12A=
XM_011529373.2:c.743+12A=	XP_011527675.1:n.743+12A=
XR_001754405.1:n.1817+12A=
XR_002958534.1:n.1926+12A=
NM_001282447.3:c.1706+12A=	NP_001269376.1:n.1706+12A=
NM_025220.5:c.1706+12A= MANE Select	NP_079496.1:n.1706+12A=
NM_153202.4:c.1706+12A=	NP_694882.1:n.1706+12A=