Canonical Allele Identifier: CA1158016963
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21570332_21570333delinsGA , CM000663.2:g.21570332_21570333delinsGA GRCh38
NC_000001.10:g.21896825_21896826delinsGA , CM000663.1:g.21896825_21896826delinsGA GRCh37
NC_000001.9:g.21769412_21769413delinsGA NCBI36
NG_008940.1:g.65968_65969delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000374840.8:c.820_821delinsGA MANE Select ENSP00000363973.3:p.Glu274=
ENST00000374830.2:c.30_31delinsGA
ENST00000374832.5:c.820_821delinsGA ENSP00000363965.1:p.Glu274=
ENST00000374840.7:c.820_821delinsGA ENSP00000363973.3:p.Glu274=
ENST00000539907.5:c.589_590delinsGA ENSP00000437674.1:p.Glu197=
ENST00000540617.5:c.655_656delinsGA ENSP00000442672.1:p.Glu219=
NM_000478.4:c.820_821delinsGA NP_000469.3:p.Glu274=
NM_001127501.2:c.655_656delinsGA NP_001120973.2:p.Glu219=
NM_001177520.1:c.589_590delinsGA NP_001170991.1:p.Glu197=
XM_005245818.1:c.820_821delinsGA XP_005245875.1:p.Glu274=
XM_005245820.2:c.820_821delinsGA XP_005245877.1:p.Glu274=
XM_006710546.1:c.820_821delinsGA XP_006710609.1:p.Glu274=
NM_000478.5:c.820_821delinsGA NP_000469.3:p.Glu274=
NM_001127501.3:c.655_656delinsGA NP_001120973.2:p.Glu219=
NM_001177520.2:c.589_590delinsGA NP_001170991.1:p.Glu197=
XM_006710546.3:c.820_821delinsGA XP_006710609.1:p.Glu274=
XM_017000903.1:c.664_665delinsGA XP_016856392.1:p.Glu222=
NM_000478.6:c.820_821delinsGA MANE Select NP_000469.3:p.Glu274=
NM_001127501.4:c.655_656delinsGA NP_001120973.2:p.Glu219=
NM_001177520.3:c.589_590delinsGA NP_001170991.1:p.Glu197=
NM_001369803.2:c.820_821delinsGA NP_001356732.1:p.Glu274=
NM_001369804.2:c.820_821delinsGA NP_001356733.1:p.Glu274=
NM_001369805.2:c.820_821delinsGA NP_001356734.1:p.Glu274=