Canonical Allele Identifier: CA666827

Gene: ALPL

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21577402G>A , CM000663.2:g.21577402G>A	GRCh38
NC_000001.10:g.21903895G>A , CM000663.1:g.21903895G>A	GRCh37
NC_000001.9:g.21776482G>A	NCBI36
NG_008940.1:g.73038G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.1329G>A MANE Select	ENSP00000363973.3:p.Ala443=
ENST00000374829.2:n.598G>A
ENST00000374830.2:c.404G>A
ENST00000374832.5:c.1329G>A	ENSP00000363965.1:p.Ala443=
ENST00000374840.7:c.1329G>A	ENSP00000363973.3:p.Ala443=
ENST00000539907.5:c.1098G>A	ENSP00000437674.1:p.Ala366=
ENST00000540617.5:c.1164G>A	ENSP00000442672.1:p.Ala388=
NM_000478.4:c.1329G>A	NP_000469.3:p.Ala443=
NM_001127501.2:c.1164G>A	NP_001120973.2:p.Ala388=
NM_001177520.1:c.1098G>A	NP_001170991.1:p.Ala366=
XM_005245818.1:c.1329G>A	XP_005245875.1:p.Ala443=
XM_006710546.1:c.1329G>A	XP_006710609.1:p.Ala443=
NM_000478.5:c.1329G>A	NP_000469.3:p.Ala443=
NM_001127501.3:c.1164G>A	NP_001120973.2:p.Ala388=
NM_001177520.2:c.1098G>A	NP_001170991.1:p.Ala366=
XM_006710546.3:c.1329G>A	XP_006710609.1:p.Ala443=
XM_017000903.1:c.1173G>A	XP_016856392.1:p.Ala391=
NM_000478.6:c.1329G>A MANE Select	NP_000469.3:p.Ala443=
NM_001127501.4:c.1164G>A	NP_001120973.2:p.Ala388=
NM_001177520.3:c.1098G>A	NP_001170991.1:p.Ala366=
NM_001369803.2:c.1329G>A	NP_001356732.1:p.Ala443=
NM_001369804.2:c.1329G>A	NP_001356733.1:p.Ala443=
NM_001369805.2:c.1329G>A	NP_001356734.1:p.Ala443=