Canonical Allele Identifier: CA408103412

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649617A>G (hg19) ; chr20:g.3668970A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668970A>G , CM000682.2:g.3668970A>G	GRCh38
NC_000020.10:g.3649617A>G , CM000682.1:g.3649617A>G	GRCh37
NC_000020.9:g.3597617A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2435T>C MANE Select	ENSP00000348912.3:p.Leu812Pro
ENST00000350009.6:c.2357T>C	ENSP00000322550.5:p.Leu786Pro
ENST00000356518.6:c.2435T>C	ENSP00000348912.2:p.Leu812Pro
ENST00000379861.8:c.2432T>C	ENSP00000369190.4:p.Leu811Pro
ENST00000466620.5:n.1996T>C
ENST00000483362.1:n.1358T>C
ENST00000617732.1:c.*1119T>C	ENSP00000483343.1:n.*1119T>C
ENST00000619289.4:c.2072T>C	ENSP00000484600.1:p.Leu691Pro
NM_001282447.1:c.2432T>C	NP_001269376.1:p.Leu811Pro
NM_025220.3:c.2435T>C	NP_079496.1:p.Leu812Pro
NM_153202.2:c.2357T>C	NP_694882.1:p.Leu786Pro
XM_005260843.1:c.2474T>C	XP_005260900.1:p.Leu825Pro
XM_006723639.1:c.2471T>C	XP_006723702.1:p.Leu824Pro
XM_006723640.1:c.2465T>C	XP_006723703.1:p.Leu822Pro
XM_011529366.1:c.2471T>C	XP_011527668.1:p.Leu824Pro
XM_011529367.1:c.2432T>C	XP_011527669.1:p.Leu811Pro
XM_011529368.1:c.2396T>C	XP_011527670.1:p.Leu799Pro
XM_011529373.1:c.1472T>C	XP_011527675.1:p.Leu491Pro
XR_937153.1:n.2456T>C
XR_937154.1:n.2456T>C
XR_937155.1:n.2377T>C
XR_937157.1:n.2379T>C
NM_001282447.2:c.2432T>C	NP_001269376.1:p.Leu811Pro
NM_025220.4:c.2435T>C	NP_079496.1:p.Leu812Pro
NM_153202.3:c.2357T>C	NP_694882.1:p.Leu786Pro
XM_011529373.2:c.1472T>C	XP_011527675.1:p.Leu491Pro
XR_001754405.1:n.2543T>C
XR_002958534.1:n.2652T>C
NM_001282447.3:c.2432T>C	NP_001269376.1:p.Leu811Pro
NM_025220.5:c.2435T>C MANE Select	NP_079496.1:p.Leu812Pro
NM_153202.4:c.2357T>C	NP_694882.1:p.Leu786Pro