Canonical Allele Identifier: CA2832533868
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21564081_21564083del , CM000663.2:g.21564081_21564083del GRCh38
NC_000001.10:g.21890574_21890576del , CM000663.1:g.21890574_21890576del GRCh37
NC_000001.9:g.21763161_21763163del NCBI36
NG_008940.1:g.59717_59719del

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.513_515del MANE Select ENSP00000363973.3:p.Ala172del
ENST00000374832.5:c.513_515del ENSP00000363965.1:p.Ala172del
ENST00000374840.7:c.513_515del ENSP00000363973.3:p.Ala172del
ENST00000468526.1:n.573_575del
ENST00000539907.5:c.282_284del ENSP00000437674.1:p.Ala95del
ENST00000540617.5:c.348_350del ENSP00000442672.1:p.Ala117del
NM_000478.4:c.513_515del NP_000469.3:p.Ala172del
NM_001127501.2:c.348_350del NP_001120973.2:p.Ala117del
NM_001177520.1:c.282_284del NP_001170991.1:p.Ala95del
XM_005245818.1:c.513_515del XP_005245875.1:p.Ala172del
XM_005245820.2:c.513_515del XP_005245877.1:p.Ala172del
XM_006710546.1:c.513_515del XP_006710609.1:p.Ala172del
NM_000478.5:c.513_515del NP_000469.3:p.Ala172del
NM_001127501.3:c.348_350del NP_001120973.2:p.Ala117del
NM_001177520.2:c.282_284del NP_001170991.1:p.Ala95del
XM_006710546.3:c.513_515del XP_006710609.1:p.Ala172del
XM_017000903.1:c.357_359del XP_016856392.1:p.Ala120del
NM_000478.6:c.513_515del MANE Select NP_000469.3:p.Ala172del
NM_001127501.4:c.348_350del NP_001120973.2:p.Ala117del
NM_001177520.3:c.282_284del NP_001170991.1:p.Ala95del
NM_001369803.2:c.513_515del NP_001356732.1:p.Ala172del
NM_001369804.2:c.513_515del NP_001356733.1:p.Ala172del
NM_001369805.2:c.513_515del NP_001356734.1:p.Ala172del