Canonical Allele Identifier: CA1158018430

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573950C= , CM000663.2:g.21573950C=	GRCh38
NC_000001.10:g.21900443C= , CM000663.1:g.21900443C=	GRCh37
NC_000001.9:g.21773030C=	NCBI36
NG_008940.1:g.69586C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.997+151C= MANE Select	ENSP00000363973.3:n.997+151C=
ENST00000374830.2:c.73-1783C=
ENST00000374832.5:c.997+151C=	ENSP00000363965.1:n.997+151C=
ENST00000374840.7:c.997+151C=	ENSP00000363973.3:n.997+151C=
ENST00000539907.5:c.766+151C=	ENSP00000437674.1:n.766+151C=
ENST00000540617.5:c.832+151C=	ENSP00000442672.1:n.832+151C=
NM_000478.4:c.997+151C=	NP_000469.3:n.997+151C=
NM_001127501.2:c.832+151C=	NP_001120973.2:n.832+151C=
NM_001177520.1:c.766+151C=	NP_001170991.1:n.766+151C=
XM_005245818.1:c.997+151C=	XP_005245875.1:n.997+151C=
XM_005245820.2:c.998-92C=	XP_005245877.1:n.998-92C=
XM_006710546.1:c.997+151C=	XP_006710609.1:n.997+151C=
NM_000478.5:c.997+151C=	NP_000469.3:n.997+151C=
NM_001127501.3:c.832+151C=	NP_001120973.2:n.832+151C=
NM_001177520.2:c.766+151C=	NP_001170991.1:n.766+151C=
XM_006710546.3:c.997+151C=	XP_006710609.1:n.997+151C=
XM_017000903.1:c.841+151C=	XP_016856392.1:n.841+151C=
NM_000478.6:c.997+151C= MANE Select	NP_000469.3:n.997+151C=
NM_001127501.4:c.832+151C=	NP_001120973.2:n.832+151C=
NM_001177520.3:c.766+151C=	NP_001170991.1:n.766+151C=
NM_001369803.2:c.997+151C=	NP_001356732.1:n.997+151C=
NM_001369804.2:c.997+151C=	NP_001356733.1:n.997+151C=
NM_001369805.2:c.997+151C=	NP_001356734.1:n.997+151C=