Canonical Allele Identifier: CA1141580646

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21575736G= , CM000663.2:g.21575736G=	GRCh38
NC_000001.10:g.21902229G= , CM000663.1:g.21902229G=	GRCh37
NC_000001.9:g.21774816G=	NCBI36
NG_008940.1:g.71372G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.1001G= MANE Select	ENSP00000363973.3:p.Gly334=
ENST00000374829.2:n.270G=
ENST00000374830.2:c.76G=
ENST00000374832.5:c.1001G=	ENSP00000363965.1:p.Gly334=
ENST00000374840.7:c.1001G=	ENSP00000363973.3:p.Gly334=
ENST00000539907.5:c.770G=	ENSP00000437674.1:p.Gly257=
ENST00000540617.5:c.836G=	ENSP00000442672.1:p.Gly279=
NM_000478.4:c.1001G=	NP_000469.3:p.Gly334=
NM_001127501.2:c.836G=	NP_001120973.2:p.Gly279=
NM_001177520.1:c.770G=	NP_001170991.1:p.Gly257=
XM_005245818.1:c.1001G=	XP_005245875.1:p.Gly334=
XM_006710546.1:c.1001G=	XP_006710609.1:p.Gly334=
NM_000478.5:c.1001G=	NP_000469.3:p.Gly334=
NM_001127501.3:c.836G=	NP_001120973.2:p.Gly279=
NM_001177520.2:c.770G=	NP_001170991.1:p.Gly257=
XM_006710546.3:c.1001G=	XP_006710609.1:p.Gly334=
XM_017000903.1:c.845G=	XP_016856392.1:p.Gly282=
NM_000478.6:c.1001G= MANE Select	NP_000469.3:p.Gly334=
NM_001127501.4:c.836G=	NP_001120973.2:p.Gly279=
NM_001177520.3:c.770G=	NP_001170991.1:p.Gly257=
NM_001369803.2:c.1001G=	NP_001356732.1:p.Gly334=
NM_001369804.2:c.1001G=	NP_001356733.1:p.Gly334=
NM_001369805.2:c.1001G=	NP_001356734.1:p.Gly334=