Canonical Allele Identifier: CA416527789

Gene: ALPL

Linked Data

• MyVariant Identifiers: chr1:g.21890592C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21564099C>T , CM000663.2:g.21564099C>T	GRCh38
NC_000001.10:g.21890592C>T , CM000663.1:g.21890592C>T	GRCh37
NC_000001.9:g.21763179C>T	NCBI36
NG_008940.1:g.59735C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.531C>T MANE Select	ENSP00000363973.3:p.Ala177=
ENST00000374832.5:c.531C>T	ENSP00000363965.1:p.Ala177=
ENST00000374840.7:c.531C>T	ENSP00000363973.3:p.Ala177=
ENST00000468526.1:n.591C>T
ENST00000539907.5:c.300C>T	ENSP00000437674.1:p.Ala100=
ENST00000540617.5:c.366C>T	ENSP00000442672.1:p.Ala122=
NM_000478.4:c.531C>T	NP_000469.3:p.Ala177=
NM_001127501.2:c.366C>T	NP_001120973.2:p.Ala122=
NM_001177520.1:c.300C>T	NP_001170991.1:p.Ala100=
XM_005245818.1:c.531C>T	XP_005245875.1:p.Ala177=
XM_005245820.2:c.531C>T	XP_005245877.1:p.Ala177=
XM_006710546.1:c.531C>T	XP_006710609.1:p.Ala177=
NM_000478.5:c.531C>T	NP_000469.3:p.Ala177=
NM_001127501.3:c.366C>T	NP_001120973.2:p.Ala122=
NM_001177520.2:c.300C>T	NP_001170991.1:p.Ala100=
XM_006710546.3:c.531C>T	XP_006710609.1:p.Ala177=
XM_017000903.1:c.375C>T	XP_016856392.1:p.Ala125=
NM_000478.6:c.531C>T MANE Select	NP_000469.3:p.Ala177=
NM_001127501.4:c.366C>T	NP_001120973.2:p.Ala122=
NM_001177520.3:c.300C>T	NP_001170991.1:p.Ala100=
NM_001369803.2:c.531C>T	NP_001356732.1:p.Ala177=
NM_001369804.2:c.531C>T	NP_001356733.1:p.Ala177=
NM_001369805.2:c.531C>T	NP_001356734.1:p.Ala177=