Canonical Allele Identifier: CA1145196812
Gene: ALPL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.21560711C= , CM000663.2:g.21560711C= GRCh38
NC_000001.10:g.21887204C= , CM000663.1:g.21887204C= GRCh37
NC_000001.9:g.21759791C= NCBI36
NG_008940.1:g.56347C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374840.8:c.147C= MANE Select ENSP00000363973.3:p.Asn49=
ENST00000374832.5:c.147C= ENSP00000363965.1:p.Asn49=
ENST00000374840.7:c.147C= ENSP00000363973.3:p.Asn49=
ENST00000468526.1:n.207C=
ENST00000539907.5:c.32C= ENSP00000437674.1:p.Thr11=
ENST00000540617.5:c.-19C= ENSP00000442672.1:n.-19C=
NM_000478.4:c.147C= NP_000469.3:p.Asn49=
NM_001127501.2:c.-19C= NP_001120973.2:n.-19C=
NM_001177520.1:c.32C= NP_001170991.1:p.Thr11=
XM_005245818.1:c.147C= XP_005245875.1:p.Asn49=
XM_005245820.2:c.147C= XP_005245877.1:p.Asn49=
XM_006710546.1:c.147C= XP_006710609.1:p.Asn49=
NM_000478.5:c.147C= NP_000469.3:p.Asn49=
NM_001127501.3:c.-19C= NP_001120973.2:n.-19C=
NM_001177520.2:c.32C= NP_001170991.1:p.Thr11=
XM_006710546.3:c.147C= XP_006710609.1:p.Asn49=
XM_017000903.1:c.32C= XP_016856392.1:p.Thr11=
NM_000478.6:c.147C= MANE Select NP_000469.3:p.Asn49=
NM_001127501.4:c.-19C= NP_001120973.2:n.-19C=
NM_001177520.3:c.32C= NP_001170991.1:p.Thr11=
NM_001369803.2:c.147C= NP_001356732.1:p.Asn49=
NM_001369804.2:c.147C= NP_001356733.1:p.Asn49=
NM_001369805.2:c.147C= NP_001356734.1:p.Asn49=