Canonical Allele Identifier: CA2346678771

Gene: ADAM33

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3671622G= , CM000682.2:g.3671622G=	GRCh38
NC_000020.10:g.3652269G= , CM000682.1:g.3652269G=	GRCh37
NC_000020.9:g.3600269G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356518.7:c.1864C= MANE Select	ENSP00000348912.3:p.Leu622=
ENST00000350009.6:c.1864C=	ENSP00000322550.5:p.Leu622=
ENST00000356518.6:c.1864C=	ENSP00000348912.2:p.Leu622=
ENST00000379861.8:c.1864C=	ENSP00000369190.4:p.Leu622=
ENST00000466620.5:n.1503C=
ENST00000617732.1:c.*632-165C=	ENSP00000483343.1:n.*632-165C=
ENST00000619289.4:c.1504C=	ENSP00000484600.1:p.Leu502=
NM_001282447.1:c.1864C=	NP_001269376.1:p.Leu622=
NM_025220.3:c.1864C=	NP_079496.1:p.Leu622=
NM_153202.2:c.1864C=	NP_694882.1:p.Leu622=
XM_005260843.1:c.1903C=	XP_005260900.1:p.Leu635=
XM_006723639.1:c.1903C=	XP_006723702.1:p.Leu635=
XM_006723640.1:c.1894C=	XP_006723703.1:p.Leu632=
XM_011529366.1:c.1900C=	XP_011527668.1:p.Leu634=
XM_011529367.1:c.1861C=	XP_011527669.1:p.Leu621=
XM_011529368.1:c.1903C=	XP_011527670.1:p.Leu635=
XM_011529369.1:c.1871C=	XP_011527671.1:p.Pro624=
XM_011529370.1:c.1871C=	XP_011527672.1:p.Pro624=
XM_011529373.1:c.901C=	XP_011527675.1:p.Leu301=
XR_937151.1:n.2007C=
XR_937152.1:n.2007C=
XR_937153.1:n.1888C=
XR_937154.1:n.1888C=
XR_937155.1:n.1809C=
XR_937157.1:n.1811C=
NM_001282447.2:c.1864C=	NP_001269376.1:p.Leu622=
NM_025220.4:c.1864C=	NP_079496.1:p.Leu622=
NM_153202.3:c.1864C=	NP_694882.1:p.Leu622=
XM_011529373.2:c.901C=	XP_011527675.1:p.Leu301=
XR_001754405.1:n.1975C=
XR_002958534.1:n.2084C=
NM_001282447.3:c.1864C=	NP_001269376.1:p.Leu622=
NM_025220.5:c.1864C= MANE Select	NP_079496.1:p.Leu622=
NM_153202.4:c.1864C=	NP_694882.1:p.Leu622=