Canonical Allele Identifier: CA2346678804

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671684C= , CM000682.2:g.3671684C=	GRCh38
NC_000020.10:g.3652331C= , CM000682.1:g.3652331C=	GRCh37
NC_000020.9:g.3600331C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1802G= MANE Select	ENSP00000348912.3:p.Gly601=
ENST00000350009.6:c.1802G=	ENSP00000322550.5:p.Gly601=
ENST00000356518.6:c.1802G=	ENSP00000348912.2:p.Gly601=
ENST00000379861.8:c.1802G=	ENSP00000369190.4:p.Gly601=
ENST00000466620.5:n.1441G=
ENST00000617732.1:c.*632-227G=	ENSP00000483343.1:n.*632-227G=
ENST00000619289.4:c.1442G=	ENSP00000484600.1:p.Gly481=
NM_001282447.1:c.1802G=	NP_001269376.1:p.Gly601=
NM_025220.3:c.1802G=	NP_079496.1:p.Gly601=
NM_153202.2:c.1802G=	NP_694882.1:p.Gly601=
XM_005260843.1:c.1841G=	XP_005260900.1:p.Gly614=
XM_006723639.1:c.1841G=	XP_006723702.1:p.Gly614=
XM_006723640.1:c.1832G=	XP_006723703.1:p.Gly611=
XM_011529366.1:c.1838G=	XP_011527668.1:p.Gly613=
XM_011529367.1:c.1799G=	XP_011527669.1:p.Gly600=
XM_011529368.1:c.1841G=	XP_011527670.1:p.Gly614=
XM_011529369.1:c.1809G=	XP_011527671.1:p.Trp603=
XM_011529370.1:c.1809G=	XP_011527672.1:p.Trp603=
XM_011529373.1:c.839G=	XP_011527675.1:p.Gly280=
XR_937151.1:n.1945G=
XR_937152.1:n.1945G=
XR_937153.1:n.1826G=
XR_937154.1:n.1826G=
XR_937155.1:n.1747G=
XR_937157.1:n.1749G=
NM_001282447.2:c.1802G=	NP_001269376.1:p.Gly601=
NM_025220.4:c.1802G=	NP_079496.1:p.Gly601=
NM_153202.3:c.1802G=	NP_694882.1:p.Gly601=
XM_011529373.2:c.839G=	XP_011527675.1:p.Gly280=
XR_001754405.1:n.1913G=
XR_002958534.1:n.2022G=
NM_001282447.3:c.1802G=	NP_001269376.1:p.Gly601=
NM_025220.5:c.1802G= MANE Select	NP_079496.1:p.Gly601=
NM_153202.4:c.1802G=	NP_694882.1:p.Gly601=