Canonical Allele Identifier: CA509419278

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3650281G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669634G>C , CM000682.2:g.3669634G>C	GRCh38
NC_000020.10:g.3650281G>C , CM000682.1:g.3650281G>C	GRCh37
NC_000020.9:g.3598281G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2244C>G MANE Select	ENSP00000348912.3:p.Pro748=
ENST00000350009.6:c.2166C>G	ENSP00000322550.5:p.Pro722=
ENST00000356518.6:c.2244C>G	ENSP00000348912.2:p.Pro748=
ENST00000379861.8:c.2244C>G	ENSP00000369190.4:p.Pro748=
ENST00000466620.5:n.1805C>G
ENST00000483362.1:n.992C>G
ENST00000617732.1:c.*931C>G	ENSP00000483343.1:n.*931C>G
ENST00000619289.4:c.1884C>G	ENSP00000484600.1:p.Pro628=
NM_001282447.1:c.2244C>G	NP_001269376.1:p.Pro748=
NM_025220.3:c.2244C>G	NP_079496.1:p.Pro748=
NM_153202.2:c.2166C>G	NP_694882.1:p.Pro722=
XM_005260843.1:c.2283C>G	XP_005260900.1:p.Pro761=
XM_006723639.1:c.2283C>G	XP_006723702.1:p.Pro761=
XM_006723640.1:c.2274C>G	XP_006723703.1:p.Pro758=
XM_011529366.1:c.2280C>G	XP_011527668.1:p.Pro760=
XM_011529367.1:c.2241C>G	XP_011527669.1:p.Pro747=
XM_011529368.1:c.2205C>G	XP_011527670.1:p.Pro735=
XM_011529373.1:c.1281C>G	XP_011527675.1:p.Pro427=
XR_937151.1:n.2384-264C>G
XR_937152.1:n.2384-264C>G
XR_937153.1:n.2268C>G
XR_937154.1:n.2268C>G
XR_937155.1:n.2189C>G
XR_937157.1:n.2191C>G
NM_001282447.2:c.2244C>G	NP_001269376.1:p.Pro748=
NM_025220.4:c.2244C>G	NP_079496.1:p.Pro748=
NM_153202.3:c.2166C>G	NP_694882.1:p.Pro722=
XM_011529373.2:c.1281C>G	XP_011527675.1:p.Pro427=
XR_001754405.1:n.2355C>G
XR_002958534.1:n.2464C>G
NM_001282447.3:c.2244C>G	NP_001269376.1:p.Pro748=
NM_025220.5:c.2244C>G MANE Select	NP_079496.1:p.Pro748=
NM_153202.4:c.2166C>G	NP_694882.1:p.Pro722=