Canonical Allele Identifier: CA408103585

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649989G>T (hg19) ; chr20:g.3669342G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669342G>T , CM000682.2:g.3669342G>T	GRCh38
NC_000020.10:g.3649989G>T , CM000682.1:g.3649989G>T	GRCh37
NC_000020.9:g.3597989G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2361C>A MANE Select	ENSP00000348912.3:p.Ser787Arg
ENST00000350009.6:c.2283C>A	ENSP00000322550.5:p.Ser761Arg
ENST00000356518.6:c.2361C>A	ENSP00000348912.2:p.Ser787Arg
ENST00000379861.8:c.2361C>A	ENSP00000369190.4:p.Ser787Arg
ENST00000466620.5:n.1922C>A
ENST00000483362.1:n.1284C>A
ENST00000617732.1:c.*1048C>A	ENSP00000483343.1:n.*1048C>A
ENST00000619289.4:c.2001C>A	ENSP00000484600.1:p.Ser667Arg
NM_001282447.1:c.2361C>A	NP_001269376.1:p.Ser787Arg
NM_025220.3:c.2361C>A	NP_079496.1:p.Ser787Arg
NM_153202.2:c.2283C>A	NP_694882.1:p.Ser761Arg
XM_005260843.1:c.2400C>A	XP_005260900.1:p.Ser800Arg
XM_006723639.1:c.2400C>A	XP_006723702.1:p.Ser800Arg
XM_006723640.1:c.2391C>A	XP_006723703.1:p.Ser797Arg
XM_011529366.1:c.2397C>A	XP_011527668.1:p.Ser799Arg
XM_011529367.1:c.2358C>A	XP_011527669.1:p.Ser786Arg
XM_011529368.1:c.2322C>A	XP_011527670.1:p.Ser774Arg
XM_011529373.1:c.1398C>A	XP_011527675.1:p.Ser466Arg
XR_937151.1:n.2412C>A
XR_937152.1:n.2412C>A
XR_937153.1:n.2385C>A
XR_937154.1:n.2385C>A
XR_937155.1:n.2306C>A
XR_937157.1:n.2308C>A
NM_001282447.2:c.2361C>A	NP_001269376.1:p.Ser787Arg
NM_025220.4:c.2361C>A	NP_079496.1:p.Ser787Arg
NM_153202.3:c.2283C>A	NP_694882.1:p.Ser761Arg
XM_011529373.2:c.1398C>A	XP_011527675.1:p.Ser466Arg
XR_001754405.1:n.2472C>A
XR_002958534.1:n.2581C>A
NM_001282447.3:c.2361C>A	NP_001269376.1:p.Ser787Arg
NM_025220.5:c.2361C>A MANE Select	NP_079496.1:p.Ser787Arg
NM_153202.4:c.2283C>A	NP_694882.1:p.Ser761Arg