Canonical Allele Identifier: CA16040723
Gene: ALPL HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 371313
ClinVar RCV Id: RCV000410612
dbSNP Id: rs1057517173

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21577499G>T , CM000663.2:g.21577499G>T GRCh38
NC_000001.9:g.21776579G>T NCBI36
NC_000001.10:g.21903992G>T , CM000663.1:g.21903992G>T GRCh37
NG_008940.1:g.73135G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000374829.2:n.695G>T
ENST00000374830.2:n.501G>T
ENST00000374832.5:c.1426G>T ENSP00000363965.1:p.Glu476Ter
ENST00000374840.7:c.1426G>T ENSP00000363973.3:p.Glu476Ter
ENST00000539907.5:c.1195G>T ENSP00000437674.1:p.Glu399Ter
ENST00000540617.5:c.1261G>T ENSP00000442672.1:p.Glu421Ter
NM_000478.4:c.1426G>T VV NP_000469.3:p.Glu476Ter
NM_001127501.2:c.1261G>T VV NP_001120973.2:p.Glu421Ter
NM_001177520.1:c.1195G>T VV NP_001170991.1:p.Glu399Ter
XM_005245818.1:c.1426G>T XP_005245875.1:p.Glu476Ter
XM_006710546.1:c.1426G>T XP_006710609.1:p.Glu476Ter