Canonical Allele Identifier: CA1158013263

Gene: ALPL

Linked Data

• dbSNP Id: rs1644480761

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21561214dup , CM000663.2:g.21561214dup	GRCh38
NC_000001.10:g.21887707dup , CM000663.1:g.21887707dup	GRCh37
NC_000001.9:g.21760294dup	NCBI36
NG_008940.1:g.56850dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.297+2dup MANE Select	ENSP00000363973.3:n.297+2dup
ENST00000374832.5:c.297+2dup	ENSP00000363965.1:n.297+2dup
ENST00000374840.7:c.297+2dup	ENSP00000363973.3:n.297+2dup
ENST00000468526.1:n.357+2dup
ENST00000539907.5:c.66+469dup	ENSP00000437674.1:n.66+469dup
ENST00000540617.5:c.132+2dup	ENSP00000442672.1:n.132+2dup
NM_000478.4:c.297+2dup	NP_000469.3:n.297+2dup
NM_001127501.2:c.132+2dup	NP_001120973.2:n.132+2dup
NM_001177520.1:c.66+469dup	NP_001170991.1:n.66+469dup
XM_005245818.1:c.297+2dup	XP_005245875.1:n.297+2dup
XM_005245820.2:c.297+2dup	XP_005245877.1:n.297+2dup
XM_006710546.1:c.297+2dup	XP_006710609.1:n.297+2dup
NM_000478.5:c.297+2dup	NP_000469.3:n.297+2dup
NM_001127501.3:c.132+2dup	NP_001120973.2:n.132+2dup
NM_001177520.2:c.66+469dup	NP_001170991.1:n.66+469dup
XM_006710546.3:c.297+2dup	XP_006710609.1:n.297+2dup
XM_017000903.1:c.141+2dup	XP_016856392.1:n.141+2dup
NM_000478.6:c.297+2dup MANE Select	NP_000469.3:n.297+2dup
NM_001127501.4:c.132+2dup	NP_001120973.2:n.132+2dup
NM_001177520.3:c.66+469dup	NP_001170991.1:n.66+469dup
NM_001369803.2:c.297+2dup	NP_001356732.1:n.297+2dup
NM_001369804.2:c.297+2dup	NP_001356733.1:n.297+2dup
NM_001369805.2:c.297+2dup	NP_001356734.1:n.297+2dup