Canonical Allele Identifier: CA338880215

Gene: ALPL

Linked Data

• ClinVar Variation Id: 1717170
• ClinVar RCV Id: RCV002296334
• MyVariant Identifiers: chr1:g.21900182A>C (hg19) ; chr1:g.21573689A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21573689A>C , CM000663.2:g.21573689A>C	GRCh38
NC_000001.10:g.21900182A>C , CM000663.1:g.21900182A>C	GRCh37
NC_000001.9:g.21772769A>C	NCBI36
NG_008940.1:g.69325A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.887A>C MANE Select	ENSP00000363973.3:p.Gln296Pro
ENST00000374830.2:c.73-2044A>C
ENST00000374832.5:c.887A>C	ENSP00000363965.1:p.Gln296Pro
ENST00000374840.7:c.887A>C	ENSP00000363973.3:p.Gln296Pro
ENST00000539907.5:c.656A>C	ENSP00000437674.1:p.Gln219Pro
ENST00000540617.5:c.722A>C	ENSP00000442672.1:p.Gln241Pro
NM_000478.4:c.887A>C	NP_000469.3:p.Gln296Pro
NM_001127501.2:c.722A>C	NP_001120973.2:p.Gln241Pro
NM_001177520.1:c.656A>C	NP_001170991.1:p.Gln219Pro
XM_005245818.1:c.887A>C	XP_005245875.1:p.Gln296Pro
XM_005245820.2:c.887A>C	XP_005245877.1:p.Gln296Pro
XM_006710546.1:c.887A>C	XP_006710609.1:p.Gln296Pro
NM_000478.5:c.887A>C	NP_000469.3:p.Gln296Pro
NM_001127501.3:c.722A>C	NP_001120973.2:p.Gln241Pro
NM_001177520.2:c.656A>C	NP_001170991.1:p.Gln219Pro
XM_006710546.3:c.887A>C	XP_006710609.1:p.Gln296Pro
XM_017000903.1:c.731A>C	XP_016856392.1:p.Gln244Pro
NM_000478.6:c.887A>C MANE Select	NP_000469.3:p.Gln296Pro
NM_001127501.4:c.722A>C	NP_001120973.2:p.Gln241Pro
NM_001177520.3:c.656A>C	NP_001170991.1:p.Gln219Pro
NM_001369803.2:c.887A>C	NP_001356732.1:p.Gln296Pro
NM_001369804.2:c.887A>C	NP_001356733.1:p.Gln296Pro
NM_001369805.2:c.887A>C	NP_001356734.1:p.Gln296Pro