Canonical Allele Identifier: CA1158019327
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21575873_21575874delinsTC , CM000663.2:g.21575873_21575874delinsTC GRCh38
NC_000001.10:g.21902366_21902367delinsTC , CM000663.1:g.21902366_21902367delinsTC GRCh37
NC_000001.9:g.21774953_21774954delinsTC NCBI36
NG_008940.1:g.71509_71510delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.1138_1139delinsTC MANE Select ENSP00000363973.3:p.Ser380=
ENST00000374829.2:n.407_408delinsTC
ENST00000374830.2:c.213_214delinsTC
ENST00000374832.5:c.1138_1139delinsTC ENSP00000363965.1:p.Ser380=
ENST00000374840.7:c.1138_1139delinsTC ENSP00000363973.3:p.Ser380=
ENST00000539907.5:c.907_908delinsTC ENSP00000437674.1:p.Ser303=
ENST00000540617.5:c.973_974delinsTC ENSP00000442672.1:p.Ser325=
NM_000478.4:c.1138_1139delinsTC NP_000469.3:p.Ser380=
NM_001127501.2:c.973_974delinsTC NP_001120973.2:p.Ser325=
NM_001177520.1:c.907_908delinsTC NP_001170991.1:p.Ser303=
XM_005245818.1:c.1138_1139delinsTC XP_005245875.1:p.Ser380=
XM_006710546.1:c.1138_1139delinsTC XP_006710609.1:p.Ser380=
NM_000478.5:c.1138_1139delinsTC NP_000469.3:p.Ser380=
NM_001127501.3:c.973_974delinsTC NP_001120973.2:p.Ser325=
NM_001177520.2:c.907_908delinsTC NP_001170991.1:p.Ser303=
XM_006710546.3:c.1138_1139delinsTC XP_006710609.1:p.Ser380=
XM_017000903.1:c.982_983delinsTC XP_016856392.1:p.Ser328=
NM_000478.6:c.1138_1139delinsTC MANE Select NP_000469.3:p.Ser380=
NM_001127501.4:c.973_974delinsTC NP_001120973.2:p.Ser325=
NM_001177520.3:c.907_908delinsTC NP_001170991.1:p.Ser303=
NM_001369803.2:c.1138_1139delinsTC NP_001356732.1:p.Ser380=
NM_001369804.2:c.1138_1139delinsTC NP_001356733.1:p.Ser380=
NM_001369805.2:c.1138_1139delinsTC NP_001356734.1:p.Ser380=