Canonical Allele Identifier: CA2346677577

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3669338G= , CM000682.2:g.3669338G=	GRCh38
NC_000020.10:g.3649985G= , CM000682.1:g.3649985G=	GRCh37
NC_000020.9:g.3597985G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.2365C= MANE Select	ENSP00000348912.3:p.Pro789=
ENST00000350009.6:c.2287C=	ENSP00000322550.5:p.Pro763=
ENST00000356518.6:c.2365C=	ENSP00000348912.2:p.Pro789=
ENST00000379861.8:c.2365C=	ENSP00000369190.4:p.Pro789=
ENST00000466620.5:n.1926C=
ENST00000483362.1:n.1288C=
ENST00000617732.1:c.*1052C=	ENSP00000483343.1:n.*1052C=
ENST00000619289.4:c.2005C=	ENSP00000484600.1:p.Pro669=
NM_001282447.1:c.2365C=	NP_001269376.1:p.Pro789=
NM_025220.3:c.2365C=	NP_079496.1:p.Pro789=
NM_153202.2:c.2287C=	NP_694882.1:p.Pro763=
XM_005260843.1:c.2404C=	XP_005260900.1:p.Pro802=
XM_006723639.1:c.2404C=	XP_006723702.1:p.Pro802=
XM_006723640.1:c.2395C=	XP_006723703.1:p.Pro799=
XM_011529366.1:c.2401C=	XP_011527668.1:p.Pro801=
XM_011529367.1:c.2362C=	XP_011527669.1:p.Pro788=
XM_011529368.1:c.2326C=	XP_011527670.1:p.Pro776=
XM_011529373.1:c.1402C=	XP_011527675.1:p.Pro468=
XR_937151.1:n.2416C=
XR_937152.1:n.2416C=
XR_937153.1:n.2389C=
XR_937154.1:n.2389C=
XR_937155.1:n.2310C=
XR_937157.1:n.2312C=
NM_001282447.2:c.2365C=	NP_001269376.1:p.Pro789=
NM_025220.4:c.2365C=	NP_079496.1:p.Pro789=
NM_153202.3:c.2287C=	NP_694882.1:p.Pro763=
XM_011529373.2:c.1402C=	XP_011527675.1:p.Pro468=
XR_001754405.1:n.2476C=
XR_002958534.1:n.2585C=
NM_001282447.3:c.2365C=	NP_001269376.1:p.Pro789=
NM_025220.5:c.2365C= MANE Select	NP_079496.1:p.Pro789=
NM_153202.4:c.2287C=	NP_694882.1:p.Pro763=