Canonical Allele Identifier: CA509419168

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649627T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668980T>G , CM000682.2:g.3668980T>G	GRCh38
NC_000020.10:g.3649627T>G , CM000682.1:g.3649627T>G	GRCh37
NC_000020.9:g.3597627T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2425A>C MANE Select	ENSP00000348912.3:p.Arg809=
ENST00000350009.6:c.2347A>C	ENSP00000322550.5:p.Arg783=
ENST00000356518.6:c.2425A>C	ENSP00000348912.2:p.Arg809=
ENST00000379861.8:c.2422A>C	ENSP00000369190.4:p.Arg808=
ENST00000466620.5:n.1986A>C
ENST00000483362.1:n.1348A>C
ENST00000617732.1:c.*1109A>C	ENSP00000483343.1:n.*1109A>C
ENST00000619289.4:c.2062A>C	ENSP00000484600.1:p.Arg688=
NM_001282447.1:c.2422A>C	NP_001269376.1:p.Arg808=
NM_025220.3:c.2425A>C	NP_079496.1:p.Arg809=
NM_153202.2:c.2347A>C	NP_694882.1:p.Arg783=
XM_005260843.1:c.2464A>C	XP_005260900.1:p.Arg822=
XM_006723639.1:c.2461A>C	XP_006723702.1:p.Arg821=
XM_006723640.1:c.2455A>C	XP_006723703.1:p.Arg819=
XM_011529366.1:c.2461A>C	XP_011527668.1:p.Arg821=
XM_011529367.1:c.2422A>C	XP_011527669.1:p.Arg808=
XM_011529368.1:c.2386A>C	XP_011527670.1:p.Arg796=
XM_011529373.1:c.1462A>C	XP_011527675.1:p.Arg488=
XR_937151.1:n.2476A>C
XR_937152.1:n.2473A>C
XR_937153.1:n.2446A>C
XR_937154.1:n.2446A>C
XR_937155.1:n.2367A>C
XR_937157.1:n.2369A>C
NM_001282447.2:c.2422A>C	NP_001269376.1:p.Arg808=
NM_025220.4:c.2425A>C	NP_079496.1:p.Arg809=
NM_153202.3:c.2347A>C	NP_694882.1:p.Arg783=
XM_011529373.2:c.1462A>C	XP_011527675.1:p.Arg488=
XR_001754405.1:n.2533A>C
XR_002958534.1:n.2642A>C
NM_001282447.3:c.2422A>C	NP_001269376.1:p.Arg808=
NM_025220.5:c.2425A>C MANE Select	NP_079496.1:p.Arg809=
NM_153202.4:c.2347A>C	NP_694882.1:p.Arg783=