Canonical Allele Identifier: CA1142586436
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21573591C= , CM000663.2:g.21573591C= GRCh38
NC_000001.10:g.21900084C= , CM000663.1:g.21900084C= GRCh37
NC_000001.9:g.21772671C= NCBI36
NG_008940.1:g.69227C=

Transcript Alleles

HGVS Amino-acid change
ENST00000374840.8:c.863-74C= MANE Select ENSP00000363973.3:n.863-74C=
ENST00000374830.2:c.73-2142C=
ENST00000374832.5:c.863-74C= ENSP00000363965.1:n.863-74C=
ENST00000374840.7:c.863-74C= ENSP00000363973.3:n.863-74C=
ENST00000539907.5:c.632-74C= ENSP00000437674.1:n.632-74C=
ENST00000540617.5:c.698-74C= ENSP00000442672.1:n.698-74C=
NM_000478.4:c.863-74C= NP_000469.3:n.863-74C=
NM_001127501.2:c.698-74C= NP_001120973.2:n.698-74C=
NM_001177520.1:c.632-74C= NP_001170991.1:n.632-74C=
XM_005245818.1:c.863-74C= XP_005245875.1:n.863-74C=
XM_005245820.2:c.863-74C= XP_005245877.1:n.863-74C=
XM_006710546.1:c.863-74C= XP_006710609.1:n.863-74C=
NM_000478.5:c.863-74C= NP_000469.3:n.863-74C=
NM_001127501.3:c.698-74C= NP_001120973.2:n.698-74C=
NM_001177520.2:c.632-74C= NP_001170991.1:n.632-74C=
XM_006710546.3:c.863-74C= XP_006710609.1:n.863-74C=
XM_017000903.1:c.707-74C= XP_016856392.1:n.707-74C=
NM_000478.6:c.863-74C= MANE Select NP_000469.3:n.863-74C=
NM_001127501.4:c.698-74C= NP_001120973.2:n.698-74C=
NM_001177520.3:c.632-74C= NP_001170991.1:n.632-74C=
NM_001369803.2:c.863-74C= NP_001356732.1:n.863-74C=
NM_001369804.2:c.863-74C= NP_001356733.1:n.863-74C=
NM_001369805.2:c.863-74C= NP_001356734.1:n.863-74C=