Canonical Allele Identifier: CA1158018052

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573180T= , CM000663.2:g.21573180T=	GRCh38
NC_000001.10:g.21899673T= , CM000663.1:g.21899673T=	GRCh37
NC_000001.9:g.21772260T=	NCBI36
NG_008940.1:g.68816T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.863-485T= MANE Select	ENSP00000363973.3:n.863-485T=
ENST00000374830.2:c.73-2553T=
ENST00000374832.5:c.863-485T=	ENSP00000363965.1:n.863-485T=
ENST00000374840.7:c.863-485T=	ENSP00000363973.3:n.863-485T=
ENST00000539907.5:c.632-485T=	ENSP00000437674.1:n.632-485T=
ENST00000540617.5:c.698-485T=	ENSP00000442672.1:n.698-485T=
NM_000478.4:c.863-485T=	NP_000469.3:n.863-485T=
NM_001127501.2:c.698-485T=	NP_001120973.2:n.698-485T=
NM_001177520.1:c.632-485T=	NP_001170991.1:n.632-485T=
XM_005245818.1:c.863-485T=	XP_005245875.1:n.863-485T=
XM_005245820.2:c.863-485T=	XP_005245877.1:n.863-485T=
XM_006710546.1:c.863-485T=	XP_006710609.1:n.863-485T=
NM_000478.5:c.863-485T=	NP_000469.3:n.863-485T=
NM_001127501.3:c.698-485T=	NP_001120973.2:n.698-485T=
NM_001177520.2:c.632-485T=	NP_001170991.1:n.632-485T=
XM_006710546.3:c.863-485T=	XP_006710609.1:n.863-485T=
XM_017000903.1:c.707-485T=	XP_016856392.1:n.707-485T=
NM_000478.6:c.863-485T= MANE Select	NP_000469.3:n.863-485T=
NM_001127501.4:c.698-485T=	NP_001120973.2:n.698-485T=
NM_001177520.3:c.632-485T=	NP_001170991.1:n.632-485T=
NM_001369803.2:c.863-485T=	NP_001356732.1:n.863-485T=
NM_001369804.2:c.863-485T=	NP_001356733.1:n.863-485T=
NM_001369805.2:c.863-485T=	NP_001356734.1:n.863-485T=