Canonical Allele Identifier: CA509559953

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3651745T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671098T>G , CM000682.2:g.3671098T>G	GRCh38
NC_000020.10:g.3651745T>G , CM000682.1:g.3651745T>G	GRCh37
NC_000020.9:g.3599745T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2148A>C MANE Select	ENSP00000348912.3:p.Pro716=
ENST00000350009.6:c.2070A>C	ENSP00000322550.5:p.Pro690=
ENST00000356518.6:c.2148A>C	ENSP00000348912.2:p.Pro716=
ENST00000379861.8:c.2148A>C	ENSP00000369190.4:p.Pro716=
ENST00000466620.5:n.1709A>C
ENST00000617732.1:c.*835A>C	ENSP00000483343.1:n.*835A>C
ENST00000619289.4:c.1788A>C	ENSP00000484600.1:p.Pro596=
NM_001282447.1:c.2148A>C	NP_001269376.1:p.Pro716=
NM_025220.3:c.2148A>C	NP_079496.1:p.Pro716=
NM_153202.2:c.2070A>C	NP_694882.1:p.Pro690=
XM_005260843.1:c.2187A>C	XP_005260900.1:p.Pro729=
XM_006723639.1:c.2187A>C	XP_006723702.1:p.Pro729=
XM_006723640.1:c.2178A>C	XP_006723703.1:p.Pro726=
XM_011529366.1:c.2184A>C	XP_011527668.1:p.Pro728=
XM_011529367.1:c.2145A>C	XP_011527669.1:p.Pro715=
XM_011529368.1:c.2109A>C	XP_011527670.1:p.Pro703=
XM_011529373.1:c.1185A>C	XP_011527675.1:p.Pro395=
XR_937151.1:n.2291A>C
XR_937152.1:n.2291A>C
XR_937153.1:n.2172A>C
XR_937154.1:n.2172A>C
XR_937155.1:n.2093A>C
XR_937157.1:n.2095A>C
NM_001282447.2:c.2148A>C	NP_001269376.1:p.Pro716=
NM_025220.4:c.2148A>C	NP_079496.1:p.Pro716=
NM_153202.3:c.2070A>C	NP_694882.1:p.Pro690=
XM_011529373.2:c.1185A>C	XP_011527675.1:p.Pro395=
XR_001754405.1:n.2259A>C
XR_002958534.1:n.2368A>C
NM_001282447.3:c.2148A>C	NP_001269376.1:p.Pro716=
NM_025220.5:c.2148A>C MANE Select	NP_079496.1:p.Pro716=
NM_153202.4:c.2070A>C	NP_694882.1:p.Pro690=