Canonical Allele Identifier: CA1158014482
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21564152A= , CM000663.2:g.21564152A= GRCh38
NC_000001.10:g.21890645A= , CM000663.1:g.21890645A= GRCh37
NC_000001.9:g.21763232A= NCBI36
NG_008940.1:g.59788A=

Transcript Alleles

HGVS Amino-acid change
ENST00000374840.8:c.584A= MANE Select ENSP00000363973.3:p.Glu195=
ENST00000374832.5:c.584A= ENSP00000363965.1:p.Glu195=
ENST00000374840.7:c.584A= ENSP00000363973.3:p.Glu195=
ENST00000468526.1:n.644A=
ENST00000539907.5:c.353A= ENSP00000437674.1:p.Glu118=
ENST00000540617.5:c.419A= ENSP00000442672.1:p.Glu140=
NM_000478.4:c.584A= NP_000469.3:p.Glu195=
NM_001127501.2:c.419A= NP_001120973.2:p.Glu140=
NM_001177520.1:c.353A= NP_001170991.1:p.Glu118=
XM_005245818.1:c.584A= XP_005245875.1:p.Glu195=
XM_005245820.2:c.584A= XP_005245877.1:p.Glu195=
XM_006710546.1:c.584A= XP_006710609.1:p.Glu195=
NM_000478.5:c.584A= NP_000469.3:p.Glu195=
NM_001127501.3:c.419A= NP_001120973.2:p.Glu140=
NM_001177520.2:c.353A= NP_001170991.1:p.Glu118=
XM_006710546.3:c.584A= XP_006710609.1:p.Glu195=
XM_017000903.1:c.428A= XP_016856392.1:p.Glu143=
NM_000478.6:c.584A= MANE Select NP_000469.3:p.Glu195=
NM_001127501.4:c.419A= NP_001120973.2:p.Glu140=
NM_001177520.3:c.353A= NP_001170991.1:p.Glu118=
NM_001369803.2:c.584A= NP_001356732.1:p.Glu195=
NM_001369804.2:c.584A= NP_001356733.1:p.Glu195=
NM_001369805.2:c.584A= NP_001356734.1:p.Glu195=