Canonical Allele Identifier: CA2346677022

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668274A= , CM000682.2:g.3668274A=	GRCh38
NC_000020.10:g.3648921A= , CM000682.1:g.3648921A=	GRCh37
NC_000020.9:g.3596921A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.*689T= MANE Select	ENSP00000348912.3:n.*689T=
ENST00000350009.6:c.*689T=	ENSP00000322550.5:n.*689T=
ENST00000356518.6:c.*689T=	ENSP00000348912.2:n.*689T=
ENST00000379861.8:c.*689T=	ENSP00000369190.4:n.*689T=
ENST00000466620.5:n.2692T=
ENST00000483362.1:n.2054T=
ENST00000619289.4:c.*689T=	ENSP00000484600.1:n.*689T=
NM_001282447.1:c.*689T=	NP_001269376.1:n.*689T=
NM_025220.3:c.*689T=	NP_079496.1:n.*689T=
NM_153202.2:c.*689T=	NP_694882.1:n.*689T=
XM_005260843.1:c.*689T=	XP_005260900.1:n.*689T=
XM_006723639.1:c.*689T=	XP_006723702.1:n.*689T=
XM_006723640.1:c.*689T=	XP_006723703.1:n.*689T=
XM_011529366.1:c.*689T=	XP_011527668.1:n.*689T=
XM_011529367.1:c.*689T=	XP_011527669.1:n.*689T=
XM_011529368.1:c.*689T=	XP_011527670.1:n.*689T=
XM_011529373.1:c.*689T=	XP_011527675.1:n.*689T=
XR_937153.1:n.3152T=
XR_937154.1:n.3152T=
XR_937155.1:n.3073T=
XR_937157.1:n.3075T=
NM_001282447.2:c.*689T=	NP_001269376.1:n.*689T=
NM_025220.4:c.*689T=	NP_079496.1:n.*689T=
NM_153202.3:c.*689T=	NP_694882.1:n.*689T=
XM_011529373.2:c.*689T=	XP_011527675.1:n.*689T=
XR_001754405.1:n.3239T=
XR_002958534.1:n.3348T=
NM_001282447.3:c.*689T=	NP_001269376.1:n.*689T=
NM_025220.5:c.*689T= MANE Select	NP_079496.1:n.*689T=
NM_153202.4:c.*689T=	NP_694882.1:n.*689T=