Canonical Allele Identifier: CA408103408

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649615A>C (hg19) ; chr20:g.3668968A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3668968A>C , CM000682.2:g.3668968A>C	GRCh38
NC_000020.10:g.3649615A>C , CM000682.1:g.3649615A>C	GRCh37
NC_000020.9:g.3597615A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2437T>G MANE Select	ENSP00000348912.3:p.Trp813Gly
ENST00000350009.6:c.2359T>G	ENSP00000322550.5:p.Trp787Gly
ENST00000356518.6:c.2437T>G	ENSP00000348912.2:p.Trp813Gly
ENST00000379861.8:c.2434T>G	ENSP00000369190.4:p.Trp812Gly
ENST00000466620.5:n.1998T>G
ENST00000483362.1:n.1360T>G
ENST00000617732.1:c.*1121T>G	ENSP00000483343.1:n.*1121T>G
ENST00000619289.4:c.2074T>G	ENSP00000484600.1:p.Trp692Gly
NM_001282447.1:c.2434T>G	NP_001269376.1:p.Trp812Gly
NM_025220.3:c.2437T>G	NP_079496.1:p.Trp813Gly
NM_153202.2:c.2359T>G	NP_694882.1:p.Trp787Gly
XM_005260843.1:c.2476T>G	XP_005260900.1:p.Trp826Gly
XM_006723639.1:c.2473T>G	XP_006723702.1:p.Trp825Gly
XM_006723640.1:c.2467T>G	XP_006723703.1:p.Trp823Gly
XM_011529366.1:c.2473T>G	XP_011527668.1:p.Trp825Gly
XM_011529367.1:c.2434T>G	XP_011527669.1:p.Trp812Gly
XM_011529368.1:c.2398T>G	XP_011527670.1:p.Trp800Gly
XM_011529373.1:c.1474T>G	XP_011527675.1:p.Trp492Gly
XR_937153.1:n.2458T>G
XR_937154.1:n.2458T>G
XR_937155.1:n.2379T>G
XR_937157.1:n.2381T>G
NM_001282447.2:c.2434T>G	NP_001269376.1:p.Trp812Gly
NM_025220.4:c.2437T>G	NP_079496.1:p.Trp813Gly
NM_153202.3:c.2359T>G	NP_694882.1:p.Trp787Gly
XM_011529373.2:c.1474T>G	XP_011527675.1:p.Trp492Gly
XR_001754405.1:n.2545T>G
XR_002958534.1:n.2654T>G
NM_001282447.3:c.2434T>G	NP_001269376.1:p.Trp812Gly
NM_025220.5:c.2437T>G MANE Select	NP_079496.1:p.Trp813Gly
NM_153202.4:c.2359T>G	NP_694882.1:p.Trp787Gly