Canonical Allele Identifier: CA408103583

Gene: ADAM33

Linked Data

• MyVariant Identifiers: chr20:g.3649988G>T (hg19) ; chr20:g.3669341G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669341G>T , CM000682.2:g.3669341G>T	GRCh38
NC_000020.10:g.3649988G>T , CM000682.1:g.3649988G>T	GRCh37
NC_000020.9:g.3597988G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000356518.7:c.2362C>A MANE Select	ENSP00000348912.3:p.His788Asn
ENST00000350009.6:c.2284C>A	ENSP00000322550.5:p.His762Asn
ENST00000356518.6:c.2362C>A	ENSP00000348912.2:p.His788Asn
ENST00000379861.8:c.2362C>A	ENSP00000369190.4:p.His788Asn
ENST00000466620.5:n.1923C>A
ENST00000483362.1:n.1285C>A
ENST00000617732.1:c.*1049C>A	ENSP00000483343.1:n.*1049C>A
ENST00000619289.4:c.2002C>A	ENSP00000484600.1:p.His668Asn
NM_001282447.1:c.2362C>A	NP_001269376.1:p.His788Asn
NM_025220.3:c.2362C>A	NP_079496.1:p.His788Asn
NM_153202.2:c.2284C>A	NP_694882.1:p.His762Asn
XM_005260843.1:c.2401C>A	XP_005260900.1:p.His801Asn
XM_006723639.1:c.2401C>A	XP_006723702.1:p.His801Asn
XM_006723640.1:c.2392C>A	XP_006723703.1:p.His798Asn
XM_011529366.1:c.2398C>A	XP_011527668.1:p.His800Asn
XM_011529367.1:c.2359C>A	XP_011527669.1:p.His787Asn
XM_011529368.1:c.2323C>A	XP_011527670.1:p.His775Asn
XM_011529373.1:c.1399C>A	XP_011527675.1:p.His467Asn
XR_937151.1:n.2413C>A
XR_937152.1:n.2413C>A
XR_937153.1:n.2386C>A
XR_937154.1:n.2386C>A
XR_937155.1:n.2307C>A
XR_937157.1:n.2309C>A
NM_001282447.2:c.2362C>A	NP_001269376.1:p.His788Asn
NM_025220.4:c.2362C>A	NP_079496.1:p.His788Asn
NM_153202.3:c.2284C>A	NP_694882.1:p.His762Asn
XM_011529373.2:c.1399C>A	XP_011527675.1:p.His467Asn
XR_001754405.1:n.2473C>A
XR_002958534.1:n.2582C>A
NM_001282447.3:c.2362C>A	NP_001269376.1:p.His788Asn
NM_025220.5:c.2362C>A MANE Select	NP_079496.1:p.His788Asn
NM_153202.4:c.2284C>A	NP_694882.1:p.His762Asn