Canonical Allele Identifier: CA338881057
Gene: ALPL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21575772A>T , CM000663.2:g.21575772A>T GRCh38
NC_000001.10:g.21902265A>T , CM000663.1:g.21902265A>T GRCh37
NC_000001.9:g.21774852A>T NCBI36
NG_008940.1:g.71408A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374840.8:c.1037A>T MANE Select ENSP00000363973.3:p.Lys346Met
ENST00000374829.2:n.306A>T
ENST00000374830.2:c.112A>T
ENST00000374832.5:c.1037A>T ENSP00000363965.1:p.Lys346Met
ENST00000374840.7:c.1037A>T ENSP00000363973.3:p.Lys346Met
ENST00000539907.5:c.806A>T ENSP00000437674.1:p.Lys269Met
ENST00000540617.5:c.872A>T ENSP00000442672.1:p.Lys291Met
NM_000478.4:c.1037A>T NP_000469.3:p.Lys346Met
NM_001127501.2:c.872A>T NP_001120973.2:p.Lys291Met
NM_001177520.1:c.806A>T NP_001170991.1:p.Lys269Met
XM_005245818.1:c.1037A>T XP_005245875.1:p.Lys346Met
XM_006710546.1:c.1037A>T XP_006710609.1:p.Lys346Met
NM_000478.5:c.1037A>T NP_000469.3:p.Lys346Met
NM_001127501.3:c.872A>T NP_001120973.2:p.Lys291Met
NM_001177520.2:c.806A>T NP_001170991.1:p.Lys269Met
XM_006710546.3:c.1037A>T XP_006710609.1:p.Lys346Met
XM_017000903.1:c.881A>T XP_016856392.1:p.Lys294Met
NM_000478.6:c.1037A>T MANE Select NP_000469.3:p.Lys346Met
NM_001127501.4:c.872A>T NP_001120973.2:p.Lys291Met
NM_001177520.3:c.806A>T NP_001170991.1:p.Lys269Met
NM_001369803.2:c.1037A>T NP_001356732.1:p.Lys346Met
NM_001369804.2:c.1037A>T NP_001356733.1:p.Lys346Met
NM_001369805.2:c.1037A>T NP_001356734.1:p.Lys346Met