Canonical Allele Identifier: CA1158014012
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21563141_21563150delinsGTGCCGGCAC , CM000663.2:g.21563141_21563150delinsGTGCCGGCAC GRCh38
NC_000001.10:g.21889634_21889643delinsGTGCCGGCAC , CM000663.1:g.21889634_21889643delinsGTGCCGGCAC GRCh37
NC_000001.9:g.21762221_21762230delinsGTGCCGGCAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.329_338delinsGTGCCGGCAC MANE Select ENSP00000363973.3:p.Ser110=
ENST00000374832.5:c.329_338delinsGTGCCGGCAC ENSP00000363965.1:p.Ser110=
ENST00000374840.7:c.329_338delinsGTGCCGGCAC ENSP00000363973.3:p.Ser110=
ENST00000468526.1:n.389_398delinsGTGCCGGCAC
ENST00000539907.5:c.98_107delinsGTGCCGGCAC ENSP00000437674.1:p.Ser33=
ENST00000540617.5:c.164_173delinsGTGCCGGCAC ENSP00000442672.1:p.Ser55=
XM_005245818.1:c.329_338delinsGTGCCGGCAC XP_005245875.1:p.Ser110=
XM_005245820.2:c.329_338delinsGTGCCGGCAC XP_005245877.1:p.Ser110=
XM_006710546.1:c.329_338delinsGTGCCGGCAC XP_006710609.1:p.Ser110=
XM_006710546.3:c.329_338delinsGTGCCGGCAC XP_006710609.1:p.Ser110=
XM_017000903.1:c.173_182delinsGTGCCGGCAC XP_016856392.1:p.Ser58=
NM_000478.6:c.329_338delinsGTGCCGGCAC MANE Select NP_000469.3:p.Ser110=
NM_001127501.4:c.164_173delinsGTGCCGGCAC NP_001120973.2:p.Ser55=
NM_001177520.3:c.98_107delinsGTGCCGGCAC NP_001170991.1:p.Ser33=
NM_001369803.2:c.329_338delinsGTGCCGGCAC NP_001356732.1:p.Ser110=
NM_001369804.2:c.329_338delinsGTGCCGGCAC NP_001356733.1:p.Ser110=
NM_001369805.2:c.329_338delinsGTGCCGGCAC NP_001356734.1:p.Ser110=