Canonical Allele Identifier: CA416532964

Gene: ALPL

Linked Data

• ClinVar Variation Id: 1142800
• ClinVar RCV Id: RCV001480718
• dbSNP Id: rs1644720046
• MyVariant Identifiers: chr1:g.21902273C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21575780C>T , CM000663.2:g.21575780C>T	GRCh38
NC_000001.10:g.21902273C>T , CM000663.1:g.21902273C>T	GRCh37
NC_000001.9:g.21774860C>T	NCBI36
NG_008940.1:g.71416C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.1045C>T MANE Select	ENSP00000363973.3:p.Leu349=
ENST00000374829.2:n.314C>T
ENST00000374830.2:c.120C>T
ENST00000374832.5:c.1045C>T	ENSP00000363965.1:p.Leu349=
ENST00000374840.7:c.1045C>T	ENSP00000363973.3:p.Leu349=
ENST00000539907.5:c.814C>T	ENSP00000437674.1:p.Leu272=
ENST00000540617.5:c.880C>T	ENSP00000442672.1:p.Leu294=
NM_000478.4:c.1045C>T	NP_000469.3:p.Leu349=
NM_001127501.2:c.880C>T	NP_001120973.2:p.Leu294=
NM_001177520.1:c.814C>T	NP_001170991.1:p.Leu272=
XM_005245818.1:c.1045C>T	XP_005245875.1:p.Leu349=
XM_006710546.1:c.1045C>T	XP_006710609.1:p.Leu349=
NM_000478.5:c.1045C>T	NP_000469.3:p.Leu349=
NM_001127501.3:c.880C>T	NP_001120973.2:p.Leu294=
NM_001177520.2:c.814C>T	NP_001170991.1:p.Leu272=
XM_006710546.3:c.1045C>T	XP_006710609.1:p.Leu349=
XM_017000903.1:c.889C>T	XP_016856392.1:p.Leu297=
NM_000478.6:c.1045C>T MANE Select	NP_000469.3:p.Leu349=
NM_001127501.4:c.880C>T	NP_001120973.2:p.Leu294=
NM_001177520.3:c.814C>T	NP_001170991.1:p.Leu272=
NM_001369803.2:c.1045C>T	NP_001356732.1:p.Leu349=
NM_001369804.2:c.1045C>T	NP_001356733.1:p.Leu349=
NM_001369805.2:c.1045C>T	NP_001356734.1:p.Leu349=