Canonical Allele Identifier: CA666877

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21577615G>T , CM000663.2:g.21577615G>T	GRCh38
NC_000001.10:g.21904108G>T , CM000663.1:g.21904108G>T	GRCh37
NC_000001.9:g.21776695G>T	NCBI36
NG_008940.1:g.73251G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.1542G>T MANE Select	ENSP00000363973.3:p.Ala514=
ENST00000374829.2:n.811G>T
ENST00000374830.2:c.617G>T
ENST00000374832.5:c.1542G>T	ENSP00000363965.1:p.Ala514=
ENST00000374840.7:c.1542G>T	ENSP00000363973.3:p.Ala514=
ENST00000539907.5:c.1311G>T	ENSP00000437674.1:p.Ala437=
ENST00000540617.5:c.1377G>T	ENSP00000442672.1:p.Ala459=
NM_000478.4:c.1542G>T	NP_000469.3:p.Ala514=
NM_001127501.2:c.1377G>T	NP_001120973.2:p.Ala459=
NM_001177520.1:c.1311G>T	NP_001170991.1:p.Ala437=
XM_005245818.1:c.1542G>T	XP_005245875.1:p.Ala514=
XM_006710546.1:c.1542G>T	XP_006710609.1:p.Ala514=
NM_000478.5:c.1542G>T	NP_000469.3:p.Ala514=
NM_001127501.3:c.1377G>T	NP_001120973.2:p.Ala459=
NM_001177520.2:c.1311G>T	NP_001170991.1:p.Ala437=
XM_006710546.3:c.1542G>T	XP_006710609.1:p.Ala514=
XM_017000903.1:c.1386G>T	XP_016856392.1:p.Ala462=
NM_000478.6:c.1542G>T MANE Select	NP_000469.3:p.Ala514=
NM_001127501.4:c.1377G>T	NP_001120973.2:p.Ala459=
NM_001177520.3:c.1311G>T	NP_001170991.1:p.Ala437=
NM_001369803.2:c.1542G>T	NP_001356732.1:p.Ala514=
NM_001369804.2:c.1542G>T	NP_001356733.1:p.Ala514=
NM_001369805.2:c.1542G>T	NP_001356734.1:p.Ala514=