Canonical Allele Identifier: CA10801860
Gene: ALPL HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1256335

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21563893G>A , CM000663.2:g.21563893G>A GRCh38
NC_000001.10:g.21890386G>A , CM000663.1:g.21890386G>A GRCh37
NC_000001.9:g.21762973G>A NCBI36
NG_008940.1:g.59529G>A

Transcript Alleles

HGVS Amino-acid change
NM_000478.4:c.473-148G>A VV NP_000469.3:p.=
NM_001127501.2:c.308-148G>A VV NP_001120973.2:p.=
NM_001177520.1:c.242-148G>A VV NP_001170991.1:p.=
XM_005245818.1:c.473-148G>A XP_005245875.1:p.=
XM_005245820.2:c.473-148G>A XP_005245877.1:p.=
XM_006710546.1:c.473-148G>A XP_006710609.1:p.=
NM_000478.5:c.473-148G>A VV NP_000469.3:p.=
NM_001127501.3:c.308-148G>A VV NP_001120973.2:p.=
NM_001177520.2:c.242-148G>A VV NP_001170991.1:p.=
XM_006710546.3:c.473-148G>A XP_006710609.1:p.=
XM_017000903.1:n.317-148G>A XP_016856392.1:p.=
NM_000478.6:c.473-148G>A VV MANE Preferred NP_000469.3:p.=
ENST00000374832.5:c.473-148G>A ENSP00000363965.1:p.=
ENST00000374840.7:c.473-148G>A ENSP00000363973.3:p.=
ENST00000468526.1:n.533-148G>A
ENST00000539907.5:c.242-148G>A ENSP00000437674.1:p.=
ENST00000540617.5:c.308-148G>A ENSP00000442672.1:p.=