Canonical Allele Identifier: CA1141580642

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21570326C= , CM000663.2:g.21570326C=	GRCh38
NC_000001.10:g.21896819C= , CM000663.1:g.21896819C=	GRCh37
NC_000001.9:g.21769406C=	NCBI36
NG_008940.1:g.65962C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.814C= MANE Select	ENSP00000363973.3:p.Arg272=
ENST00000374830.2:c.24C=
ENST00000374832.5:c.814C=	ENSP00000363965.1:p.Arg272=
ENST00000374840.7:c.814C=	ENSP00000363973.3:p.Arg272=
ENST00000539907.5:c.583C=	ENSP00000437674.1:p.Arg195=
ENST00000540617.5:c.649C=	ENSP00000442672.1:p.Arg217=
NM_000478.4:c.814C=	NP_000469.3:p.Arg272=
NM_001127501.2:c.649C=	NP_001120973.2:p.Arg217=
NM_001177520.1:c.583C=	NP_001170991.1:p.Arg195=
XM_005245818.1:c.814C=	XP_005245875.1:p.Arg272=
XM_005245820.2:c.814C=	XP_005245877.1:p.Arg272=
XM_006710546.1:c.814C=	XP_006710609.1:p.Arg272=
NM_000478.5:c.814C=	NP_000469.3:p.Arg272=
NM_001127501.3:c.649C=	NP_001120973.2:p.Arg217=
NM_001177520.2:c.583C=	NP_001170991.1:p.Arg195=
XM_006710546.3:c.814C=	XP_006710609.1:p.Arg272=
XM_017000903.1:c.658C=	XP_016856392.1:p.Arg220=
NM_000478.6:c.814C= MANE Select	NP_000469.3:p.Arg272=
NM_001127501.4:c.649C=	NP_001120973.2:p.Arg217=
NM_001177520.3:c.583C=	NP_001170991.1:p.Arg195=
NM_001369803.2:c.814C=	NP_001356732.1:p.Arg272=
NM_001369804.2:c.814C=	NP_001356733.1:p.Arg272=
NM_001369805.2:c.814C=	NP_001356734.1:p.Arg272=