Canonical Allele Identifier: CA509559849

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3652093G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671446G>T , CM000682.2:g.3671446G>T	GRCh38
NC_000020.10:g.3652093G>T , CM000682.1:g.3652093G>T	GRCh37
NC_000020.9:g.3600093G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1956C>A MANE Select	ENSP00000348912.3:p.Arg652=
ENST00000350009.6:c.1906-101C>A	ENSP00000322550.5:n.1906-101C>A
ENST00000356518.6:c.1956C>A	ENSP00000348912.2:p.Arg652=
ENST00000379861.8:c.1956C>A	ENSP00000369190.4:p.Arg652=
ENST00000466620.5:n.1545-101C>A
ENST00000617732.1:c.*643C>A	ENSP00000483343.1:n.*643C>A
ENST00000619289.4:c.1596C>A	ENSP00000484600.1:p.Arg532=
NM_001282447.1:c.1956C>A	NP_001269376.1:p.Arg652=
NM_025220.3:c.1956C>A	NP_079496.1:p.Arg652=
NM_153202.2:c.1906-101C>A	NP_694882.1:n.1906-101C>A
XM_005260843.1:c.1995C>A	XP_005260900.1:p.Arg665=
XM_006723639.1:c.1995C>A	XP_006723702.1:p.Arg665=
XM_006723640.1:c.1986C>A	XP_006723703.1:p.Arg662=
XM_011529366.1:c.1992C>A	XP_011527668.1:p.Arg664=
XM_011529367.1:c.1953C>A	XP_011527669.1:p.Arg651=
XM_011529368.1:c.1945-101C>A	XP_011527670.1:n.1945-101C>A
XM_011529369.1:c.*55C>A	XP_011527671.1:n.*55C>A
XM_011529370.1:c.*5-101C>A	XP_011527672.1:n.*5-101C>A
XM_011529373.1:c.993C>A	XP_011527675.1:p.Arg331=
XR_937151.1:n.2099C>A
XR_937152.1:n.2099C>A
XR_937153.1:n.1980C>A
XR_937154.1:n.1980C>A
XR_937155.1:n.1901C>A
XR_937157.1:n.1903C>A
NM_001282447.2:c.1956C>A	NP_001269376.1:p.Arg652=
NM_025220.4:c.1956C>A	NP_079496.1:p.Arg652=
NM_153202.3:c.1906-101C>A	NP_694882.1:n.1906-101C>A
XM_011529373.2:c.993C>A	XP_011527675.1:p.Arg331=
XR_001754405.1:n.2067C>A
XR_002958534.1:n.2176C>A
NM_001282447.3:c.1956C>A	NP_001269376.1:p.Arg652=
NM_025220.5:c.1956C>A MANE Select	NP_079496.1:p.Arg652=
NM_153202.4:c.1906-101C>A	NP_694882.1:n.1906-101C>A