Canonical Allele Identifier: CA416534130

Gene: ALPL

Linked Data

• MyVariant Identifiers: chr1:g.21887664A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21561171A>C , CM000663.2:g.21561171A>C	GRCh38
NC_000001.10:g.21887664A>C , CM000663.1:g.21887664A>C	GRCh37
NC_000001.9:g.21760251A>C	NCBI36
NG_008940.1:g.56807A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.256A>C MANE Select	ENSP00000363973.3:p.Arg86=
ENST00000374832.5:c.256A>C	ENSP00000363965.1:p.Arg86=
ENST00000374840.7:c.256A>C	ENSP00000363973.3:p.Arg86=
ENST00000468526.1:n.316A>C
ENST00000539907.5:c.66+426A>C	ENSP00000437674.1:n.66+426A>C
ENST00000540617.5:c.91A>C	ENSP00000442672.1:p.Arg31=
NM_000478.4:c.256A>C	NP_000469.3:p.Arg86=
NM_001127501.2:c.91A>C	NP_001120973.2:p.Arg31=
NM_001177520.1:c.66+426A>C	NP_001170991.1:n.66+426A>C
XM_005245818.1:c.256A>C	XP_005245875.1:p.Arg86=
XM_005245820.2:c.256A>C	XP_005245877.1:p.Arg86=
XM_006710546.1:c.256A>C	XP_006710609.1:p.Arg86=
NM_000478.5:c.256A>C	NP_000469.3:p.Arg86=
NM_001127501.3:c.91A>C	NP_001120973.2:p.Arg31=
NM_001177520.2:c.66+426A>C	NP_001170991.1:n.66+426A>C
XM_006710546.3:c.256A>C	XP_006710609.1:p.Arg86=
XM_017000903.1:c.100A>C	XP_016856392.1:p.Arg34=
NM_000478.6:c.256A>C MANE Select	NP_000469.3:p.Arg86=
NM_001127501.4:c.91A>C	NP_001120973.2:p.Arg31=
NM_001177520.3:c.66+426A>C	NP_001170991.1:n.66+426A>C
NM_001369803.2:c.256A>C	NP_001356732.1:p.Arg86=
NM_001369804.2:c.256A>C	NP_001356733.1:p.Arg86=
NM_001369805.2:c.256A>C	NP_001356734.1:p.Arg86=