Canonical Allele Identifier: CA408103538

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649967C>T (hg19) ; chr20:g.3669320C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669320C>T , CM000682.2:g.3669320C>T	GRCh38
NC_000020.10:g.3649967C>T , CM000682.1:g.3649967C>T	GRCh37
NC_000020.9:g.3597967C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2383G>A MANE Select	ENSP00000348912.3:p.Ala795Thr
ENST00000350009.6:c.2305G>A	ENSP00000322550.5:p.Ala769Thr
ENST00000356518.6:c.2383G>A	ENSP00000348912.2:p.Ala795Thr
ENST00000379861.8:c.2383G>A	ENSP00000369190.4:p.Ala795Thr
ENST00000466620.5:n.1944G>A
ENST00000483362.1:n.1306G>A
ENST00000617732.1:c.*1070G>A	ENSP00000483343.1:n.*1070G>A
ENST00000619289.4:c.2023G>A	ENSP00000484600.1:p.Ala675Thr
NM_001282447.1:c.2383G>A	NP_001269376.1:p.Ala795Thr
NM_025220.3:c.2383G>A	NP_079496.1:p.Ala795Thr
NM_153202.2:c.2305G>A	NP_694882.1:p.Ala769Thr
XM_005260843.1:c.2422G>A	XP_005260900.1:p.Ala808Thr
XM_006723639.1:c.2422G>A	XP_006723702.1:p.Ala808Thr
XM_006723640.1:c.2413G>A	XP_006723703.1:p.Ala805Thr
XM_011529366.1:c.2419G>A	XP_011527668.1:p.Ala807Thr
XM_011529367.1:c.2380G>A	XP_011527669.1:p.Ala794Thr
XM_011529368.1:c.2344G>A	XP_011527670.1:p.Ala782Thr
XM_011529373.1:c.1420G>A	XP_011527675.1:p.Ala474Thr
XR_937151.1:n.2434G>A
XR_937152.1:n.2434G>A
XR_937153.1:n.2407G>A
XR_937154.1:n.2407G>A
XR_937155.1:n.2328G>A
XR_937157.1:n.2330G>A
NM_001282447.2:c.2383G>A	NP_001269376.1:p.Ala795Thr
NM_025220.4:c.2383G>A	NP_079496.1:p.Ala795Thr
NM_153202.3:c.2305G>A	NP_694882.1:p.Ala769Thr
XM_011529373.2:c.1420G>A	XP_011527675.1:p.Ala474Thr
XR_001754405.1:n.2494G>A
XR_002958534.1:n.2603G>A
NM_001282447.3:c.2383G>A	NP_001269376.1:p.Ala795Thr
NM_025220.5:c.2383G>A MANE Select	NP_079496.1:p.Ala795Thr
NM_153202.4:c.2305G>A	NP_694882.1:p.Ala769Thr