Canonical Allele Identifier: CA509559750

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652237T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671590T>A , CM000682.2:g.3671590T>A	GRCh38
NC_000020.10:g.3652237T>A , CM000682.1:g.3652237T>A	GRCh37
NC_000020.9:g.3600237T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1896A>T MANE Select	ENSP00000348912.3:p.Gly632=
ENST00000350009.6:c.1896A>T	ENSP00000322550.5:p.Gly632=
ENST00000356518.6:c.1896A>T	ENSP00000348912.2:p.Gly632=
ENST00000379861.8:c.1896A>T	ENSP00000369190.4:p.Gly632=
ENST00000466620.5:n.1535A>T
ENST00000617732.1:c.*632-133A>T	ENSP00000483343.1:n.*632-133A>T
ENST00000619289.4:c.1536A>T	ENSP00000484600.1:p.Gly512=
NM_001282447.1:c.1896A>T	NP_001269376.1:p.Gly632=
NM_025220.3:c.1896A>T	NP_079496.1:p.Gly632=
NM_153202.2:c.1896A>T	NP_694882.1:p.Gly632=
XM_005260843.1:c.1935A>T	XP_005260900.1:p.Gly645=
XM_006723639.1:c.1935A>T	XP_006723702.1:p.Gly645=
XM_006723640.1:c.1926A>T	XP_006723703.1:p.Gly642=
XM_011529366.1:c.1932A>T	XP_011527668.1:p.Gly644=
XM_011529367.1:c.1893A>T	XP_011527669.1:p.Gly631=
XM_011529368.1:c.1935A>T	XP_011527670.1:p.Gly645=
XM_011529369.1:c.1903A>T	XP_011527671.1:p.Thr635Ser
XM_011529370.1:c.1903A>T	XP_011527672.1:p.Thr635Ser
XM_011529373.1:c.933A>T	XP_011527675.1:p.Gly311=
XR_937151.1:n.2039A>T
XR_937152.1:n.2039A>T
XR_937153.1:n.1920A>T
XR_937154.1:n.1920A>T
XR_937155.1:n.1841A>T
XR_937157.1:n.1843A>T
NM_001282447.2:c.1896A>T	NP_001269376.1:p.Gly632=
NM_025220.4:c.1896A>T	NP_079496.1:p.Gly632=
NM_153202.3:c.1896A>T	NP_694882.1:p.Gly632=
XM_011529373.2:c.933A>T	XP_011527675.1:p.Gly311=
XR_001754405.1:n.2007A>T
XR_002958534.1:n.2116A>T
NM_001282447.3:c.1896A>T	NP_001269376.1:p.Gly632=
NM_025220.5:c.1896A>T MANE Select	NP_079496.1:p.Gly632=
NM_153202.4:c.1896A>T	NP_694882.1:p.Gly632=