Canonical Allele Identifier: CA1158014438

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21564047_21564048delinsCT , CM000663.2:g.21564047_21564048delinsCT	GRCh38
NC_000001.10:g.21890540_21890541delinsCT , CM000663.1:g.21890540_21890541delinsCT	GRCh37
NC_000001.9:g.21763127_21763128delinsCT	NCBI36
NG_008940.1:g.59683_59684delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.479_480delinsCT MANE Select	ENSP00000363973.3:p.Ser160=
ENST00000374832.5:c.479_480delinsCT	ENSP00000363965.1:p.Ser160=
ENST00000374840.7:c.479_480delinsCT	ENSP00000363973.3:p.Ser160=
ENST00000468526.1:n.539_540delinsCT
ENST00000539907.5:c.248_249delinsCT	ENSP00000437674.1:p.Ser83=
ENST00000540617.5:c.314_315delinsCT	ENSP00000442672.1:p.Ser105=
NM_000478.4:c.479_480delinsCT	NP_000469.3:p.Ser160=
NM_001127501.2:c.314_315delinsCT	NP_001120973.2:p.Ser105=
NM_001177520.1:c.248_249delinsCT	NP_001170991.1:p.Ser83=
XM_005245818.1:c.479_480delinsCT	XP_005245875.1:p.Ser160=
XM_005245820.2:c.479_480delinsCT	XP_005245877.1:p.Ser160=
XM_006710546.1:c.479_480delinsCT	XP_006710609.1:p.Ser160=
NM_000478.5:c.479_480delinsCT	NP_000469.3:p.Ser160=
NM_001127501.3:c.314_315delinsCT	NP_001120973.2:p.Ser105=
NM_001177520.2:c.248_249delinsCT	NP_001170991.1:p.Ser83=
XM_006710546.3:c.479_480delinsCT	XP_006710609.1:p.Ser160=
XM_017000903.1:c.323_324delinsCT	XP_016856392.1:p.Ser108=
NM_000478.6:c.479_480delinsCT MANE Select	NP_000469.3:p.Ser160=
NM_001127501.4:c.314_315delinsCT	NP_001120973.2:p.Ser105=
NM_001177520.3:c.248_249delinsCT	NP_001170991.1:p.Ser83=
NM_001369803.2:c.479_480delinsCT	NP_001356732.1:p.Ser160=
NM_001369804.2:c.479_480delinsCT	NP_001356733.1:p.Ser160=
NM_001369805.2:c.479_480delinsCT	NP_001356734.1:p.Ser160=