Canonical Allele Identifier: CA416677810

Gene: ALPL

Linked Data

• ClinVar Variation Id: 991462
• ClinVar RCV Id: RCV001279679 ; RCV002537861
• dbSNP Id: rs1455969376
• gnomAD v2: 1-21904133-C-T
• gnomAD v4: 1-21577640-C-T
• MyVariant Identifiers: chr1:g.21904133C>T (hg19) ; chr1:g.21577640C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21577640C>T , CM000663.2:g.21577640C>T	GRCh38
NC_000001.10:g.21904133C>T , CM000663.1:g.21904133C>T	GRCh37
NC_000001.9:g.21776720C>T	NCBI36
NG_008940.1:g.73276C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.1567C>T MANE Select	ENSP00000363973.3:p.Leu523=
ENST00000374829.2:n.836C>T
ENST00000374830.2:c.642C>T
ENST00000374832.5:c.1567C>T	ENSP00000363965.1:p.Leu523=
ENST00000374840.7:c.1567C>T	ENSP00000363973.3:p.Leu523=
ENST00000539907.5:c.1336C>T	ENSP00000437674.1:p.Leu446=
ENST00000540617.5:c.1402C>T	ENSP00000442672.1:p.Leu468=
NM_000478.4:c.1567C>T	NP_000469.3:p.Leu523=
NM_001127501.2:c.1402C>T	NP_001120973.2:p.Leu468=
NM_001177520.1:c.1336C>T	NP_001170991.1:p.Leu446=
XM_005245818.1:c.1567C>T	XP_005245875.1:p.Leu523=
XM_006710546.1:c.1567C>T	XP_006710609.1:p.Leu523=
NM_000478.5:c.1567C>T	NP_000469.3:p.Leu523=
NM_001127501.3:c.1402C>T	NP_001120973.2:p.Leu468=
NM_001177520.2:c.1336C>T	NP_001170991.1:p.Leu446=
XM_006710546.3:c.1567C>T	XP_006710609.1:p.Leu523=
XM_017000903.1:c.1411C>T	XP_016856392.1:p.Leu471=
NM_000478.6:c.1567C>T MANE Select	NP_000469.3:p.Leu523=
NM_001127501.4:c.1402C>T	NP_001120973.2:p.Leu468=
NM_001177520.3:c.1336C>T	NP_001170991.1:p.Leu446=
NM_001369803.2:c.1567C>T	NP_001356732.1:p.Leu523=
NM_001369804.2:c.1567C>T	NP_001356733.1:p.Leu523=
NM_001369805.2:c.1567C>T	NP_001356734.1:p.Leu523=