Canonical Allele Identifier: CA338877117

Gene: ALPL

Linked Data

• gnomAD v3: 1-21563142-T-A
• gnomAD v4: 1-21563142-T-A
• MyVariant Identifiers: chr1:g.21889635T>A (hg19) ; chr1:g.21563142T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21563142T>A , CM000663.2:g.21563142T>A	GRCh38
NC_000001.10:g.21889635T>A , CM000663.1:g.21889635T>A	GRCh37
NC_000001.9:g.21762222T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.330T>A MANE Select	ENSP00000363973.3:p.Ser110Arg
ENST00000374832.5:c.330T>A	ENSP00000363965.1:p.Ser110Arg
ENST00000374840.7:c.330T>A	ENSP00000363973.3:p.Ser110Arg
ENST00000468526.1:n.390T>A
ENST00000539907.5:c.99T>A	ENSP00000437674.1:p.Ser33Arg
ENST00000540617.5:c.165T>A	ENSP00000442672.1:p.Ser55Arg
XM_005245818.1:c.330T>A	XP_005245875.1:p.Ser110Arg
XM_005245820.2:c.330T>A	XP_005245877.1:p.Ser110Arg
XM_006710546.1:c.330T>A	XP_006710609.1:p.Ser110Arg
XM_006710546.3:c.330T>A	XP_006710609.1:p.Ser110Arg
XM_017000903.1:c.174T>A	XP_016856392.1:p.Ser58Arg
NM_000478.6:c.330T>A MANE Select	NP_000469.3:p.Ser110Arg
NM_001127501.4:c.165T>A	NP_001120973.2:p.Ser55Arg
NM_001177520.3:c.99T>A	NP_001170991.1:p.Ser33Arg
NM_001369803.2:c.330T>A	NP_001356732.1:p.Ser110Arg
NM_001369804.2:c.330T>A	NP_001356733.1:p.Ser110Arg
NM_001369805.2:c.330T>A	NP_001356734.1:p.Ser110Arg