Canonical Allele Identifier: CA338879954

Gene: ALPL

Linked Data

• MyVariant Identifiers: chr1:g.21896840G>A (hg19) ; chr1:g.21570347G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21570347G>A , CM000663.2:g.21570347G>A	GRCh38
NC_000001.10:g.21896840G>A , CM000663.1:g.21896840G>A	GRCh37
NC_000001.9:g.21769427G>A	NCBI36
NG_008940.1:g.65983G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.835G>A MANE Select	ENSP00000363973.3:p.Asp279Asn
ENST00000374830.2:c.45G>A
ENST00000374832.5:c.835G>A	ENSP00000363965.1:p.Asp279Asn
ENST00000374840.7:c.835G>A	ENSP00000363973.3:p.Asp279Asn
ENST00000539907.5:c.604G>A	ENSP00000437674.1:p.Asp202Asn
ENST00000540617.5:c.670G>A	ENSP00000442672.1:p.Asp224Asn
NM_000478.4:c.835G>A	NP_000469.3:p.Asp279Asn
NM_001127501.2:c.670G>A	NP_001120973.2:p.Asp224Asn
NM_001177520.1:c.604G>A	NP_001170991.1:p.Asp202Asn
XM_005245818.1:c.835G>A	XP_005245875.1:p.Asp279Asn
XM_005245820.2:c.835G>A	XP_005245877.1:p.Asp279Asn
XM_006710546.1:c.835G>A	XP_006710609.1:p.Asp279Asn
NM_000478.5:c.835G>A	NP_000469.3:p.Asp279Asn
NM_001127501.3:c.670G>A	NP_001120973.2:p.Asp224Asn
NM_001177520.2:c.604G>A	NP_001170991.1:p.Asp202Asn
XM_006710546.3:c.835G>A	XP_006710609.1:p.Asp279Asn
XM_017000903.1:c.679G>A	XP_016856392.1:p.Asp227Asn
NM_000478.6:c.835G>A MANE Select	NP_000469.3:p.Asp279Asn
NM_001127501.4:c.670G>A	NP_001120973.2:p.Asp224Asn
NM_001177520.3:c.604G>A	NP_001170991.1:p.Asp202Asn
NM_001369803.2:c.835G>A	NP_001356732.1:p.Asp279Asn
NM_001369804.2:c.835G>A	NP_001356733.1:p.Asp279Asn
NM_001369805.2:c.835G>A	NP_001356734.1:p.Asp279Asn