Canonical Allele Identifier: CA1146139909

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573739G= , CM000663.2:g.21573739G=	GRCh38
NC_000001.10:g.21900232G= , CM000663.1:g.21900232G=	GRCh37
NC_000001.9:g.21772819G=	NCBI36
NG_008940.1:g.69375G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.937G= MANE Select	ENSP00000363973.3:p.Val313=
ENST00000374830.2:c.73-1994G=
ENST00000374832.5:c.937G=	ENSP00000363965.1:p.Val313=
ENST00000374840.7:c.937G=	ENSP00000363973.3:p.Val313=
ENST00000539907.5:c.706G=	ENSP00000437674.1:p.Val236=
ENST00000540617.5:c.772G=	ENSP00000442672.1:p.Val258=
NM_000478.4:c.937G=	NP_000469.3:p.Val313=
NM_001127501.2:c.772G=	NP_001120973.2:p.Val258=
NM_001177520.1:c.706G=	NP_001170991.1:p.Val236=
XM_005245818.1:c.937G=	XP_005245875.1:p.Val313=
XM_005245820.2:c.937G=	XP_005245877.1:p.Val313=
XM_006710546.1:c.937G=	XP_006710609.1:p.Val313=
NM_000478.5:c.937G=	NP_000469.3:p.Val313=
NM_001127501.3:c.772G=	NP_001120973.2:p.Val258=
NM_001177520.2:c.706G=	NP_001170991.1:p.Val236=
XM_006710546.3:c.937G=	XP_006710609.1:p.Val313=
XM_017000903.1:c.781G=	XP_016856392.1:p.Val261=
NM_000478.6:c.937G= MANE Select	NP_000469.3:p.Val313=
NM_001127501.4:c.772G=	NP_001120973.2:p.Val258=
NM_001177520.3:c.706G=	NP_001170991.1:p.Val236=
NM_001369803.2:c.937G=	NP_001356732.1:p.Val313=
NM_001369804.2:c.937G=	NP_001356733.1:p.Val313=
NM_001369805.2:c.937G=	NP_001356734.1:p.Val313=