Canonical Allele Identifier: CA338877370

Gene: ALPL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21563269T>C , CM000663.2:g.21563269T>C	GRCh38
NC_000001.10:g.21889762T>C , CM000663.1:g.21889762T>C	GRCh37
NC_000001.9:g.21762349T>C	NCBI36
NG_008940.1:g.58905T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.457T>C MANE Select	ENSP00000363973.3:p.Trp153Arg
ENST00000374832.5:c.457T>C	ENSP00000363965.1:p.Trp153Arg
ENST00000374840.7:c.457T>C	ENSP00000363973.3:p.Trp153Arg
ENST00000468526.1:n.517T>C
ENST00000539907.5:c.226T>C	ENSP00000437674.1:p.Trp76Arg
ENST00000540617.5:c.292T>C	ENSP00000442672.1:p.Trp98Arg
NM_000478.4:c.457T>C	NP_000469.3:p.Trp153Arg
NM_001127501.2:c.292T>C	NP_001120973.2:p.Trp98Arg
NM_001177520.1:c.226T>C	NP_001170991.1:p.Trp76Arg
XM_005245818.1:c.457T>C	XP_005245875.1:p.Trp153Arg
XM_005245820.2:c.457T>C	XP_005245877.1:p.Trp153Arg
XM_006710546.1:c.457T>C	XP_006710609.1:p.Trp153Arg
NM_000478.5:c.457T>C	NP_000469.3:p.Trp153Arg
NM_001127501.3:c.292T>C	NP_001120973.2:p.Trp98Arg
NM_001177520.2:c.226T>C	NP_001170991.1:p.Trp76Arg
XM_006710546.3:c.457T>C	XP_006710609.1:p.Trp153Arg
XM_017000903.1:c.301T>C	XP_016856392.1:p.Trp101Arg
NM_000478.6:c.457T>C MANE Select	NP_000469.3:p.Trp153Arg
NM_001127501.4:c.292T>C	NP_001120973.2:p.Trp98Arg
NM_001177520.3:c.226T>C	NP_001170991.1:p.Trp76Arg
NM_001369803.2:c.457T>C	NP_001356732.1:p.Trp153Arg
NM_001369804.2:c.457T>C	NP_001356733.1:p.Trp153Arg
NM_001369805.2:c.457T>C	NP_001356734.1:p.Trp153Arg