Canonical Allele Identifier: CA16040721

Gene: ALPL

Linked Data

• ClinVar Variation Id: 370603
• ClinVar RCV Id: RCV000412264 ; RCV003558360
• dbSNP Id: rs1057516622
• gnomAD v4: 1-21575731-A-G
• MyVariant Identifiers: chr1:g.21902224A>G (hg19) ; chr1:g.21575731A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21575731A>G , CM000663.2:g.21575731A>G	GRCh38
NC_000001.10:g.21902224A>G , CM000663.1:g.21902224A>G	GRCh37
NC_000001.9:g.21774811A>G	NCBI36
NG_008940.1:g.71367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.998-2A>G MANE Select	ENSP00000363973.3:n.998-2A>G
ENST00000374829.2:n.267-2A>G
ENST00000374830.2:c.73-2A>G
ENST00000374832.5:c.998-2A>G	ENSP00000363965.1:n.998-2A>G
ENST00000374840.7:c.998-2A>G	ENSP00000363973.3:n.998-2A>G
ENST00000539907.5:c.767-2A>G	ENSP00000437674.1:n.767-2A>G
ENST00000540617.5:c.833-2A>G	ENSP00000442672.1:n.833-2A>G
NM_000478.4:c.998-2A>G	NP_000469.3:n.998-2A>G
NM_001127501.2:c.833-2A>G	NP_001120973.2:n.833-2A>G
NM_001177520.1:c.767-2A>G	NP_001170991.1:n.767-2A>G
XM_005245818.1:c.998-2A>G	XP_005245875.1:n.998-2A>G
XM_006710546.1:c.998-2A>G	XP_006710609.1:n.998-2A>G
NM_000478.5:c.998-2A>G	NP_000469.3:n.998-2A>G
NM_001127501.3:c.833-2A>G	NP_001120973.2:n.833-2A>G
NM_001177520.2:c.767-2A>G	NP_001170991.1:n.767-2A>G
XM_006710546.3:c.998-2A>G	XP_006710609.1:n.998-2A>G
XM_017000903.1:c.842-2A>G	XP_016856392.1:n.842-2A>G
NM_000478.6:c.998-2A>G MANE Select	NP_000469.3:n.998-2A>G
NM_001127501.4:c.833-2A>G	NP_001120973.2:n.833-2A>G
NM_001177520.3:c.767-2A>G	NP_001170991.1:n.767-2A>G
NM_001369803.2:c.998-2A>G	NP_001356732.1:n.998-2A>G
NM_001369804.2:c.998-2A>G	NP_001356733.1:n.998-2A>G
NM_001369805.2:c.998-2A>G	NP_001356734.1:n.998-2A>G