Canonical Allele Identifier: CA509559994

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652333A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671686A>G , CM000682.2:g.3671686A>G	GRCh38
NC_000020.10:g.3652333A>G , CM000682.1:g.3652333A>G	GRCh37
NC_000020.9:g.3600333A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1800T>C MANE Select	ENSP00000348912.3:p.Asp600=
ENST00000350009.6:c.1800T>C	ENSP00000322550.5:p.Asp600=
ENST00000356518.6:c.1800T>C	ENSP00000348912.2:p.Asp600=
ENST00000379861.8:c.1800T>C	ENSP00000369190.4:p.Asp600=
ENST00000466620.5:n.1439T>C
ENST00000617732.1:c.*632-229T>C	ENSP00000483343.1:n.*632-229T>C
ENST00000619289.4:c.1440T>C	ENSP00000484600.1:p.Asp480=
NM_001282447.1:c.1800T>C	NP_001269376.1:p.Asp600=
NM_025220.3:c.1800T>C	NP_079496.1:p.Asp600=
NM_153202.2:c.1800T>C	NP_694882.1:p.Asp600=
XM_005260843.1:c.1839T>C	XP_005260900.1:p.Asp613=
XM_006723639.1:c.1839T>C	XP_006723702.1:p.Asp613=
XM_006723640.1:c.1830T>C	XP_006723703.1:p.Asp610=
XM_011529366.1:c.1836T>C	XP_011527668.1:p.Asp612=
XM_011529367.1:c.1797T>C	XP_011527669.1:p.Asp599=
XM_011529368.1:c.1839T>C	XP_011527670.1:p.Asp613=
XM_011529369.1:c.1807T>C	XP_011527671.1:p.Trp603Arg
XM_011529370.1:c.1807T>C	XP_011527672.1:p.Trp603Arg
XM_011529373.1:c.837T>C	XP_011527675.1:p.Asp279=
XR_937151.1:n.1943T>C
XR_937152.1:n.1943T>C
XR_937153.1:n.1824T>C
XR_937154.1:n.1824T>C
XR_937155.1:n.1745T>C
XR_937157.1:n.1747T>C
NM_001282447.2:c.1800T>C	NP_001269376.1:p.Asp600=
NM_025220.4:c.1800T>C	NP_079496.1:p.Asp600=
NM_153202.3:c.1800T>C	NP_694882.1:p.Asp600=
XM_011529373.2:c.837T>C	XP_011527675.1:p.Asp279=
XR_001754405.1:n.1911T>C
XR_002958534.1:n.2020T>C
NM_001282447.3:c.1800T>C	NP_001269376.1:p.Asp600=
NM_025220.5:c.1800T>C MANE Select	NP_079496.1:p.Asp600=
NM_153202.4:c.1800T>C	NP_694882.1:p.Asp600=