Canonical Allele Identifier: CA2643930027

Gene: ALPL

Linked Data

• ClinVar Variation Id: 2807380
• ClinVar RCV Id: RCV003682303
• gnomAD v4: 1-21561228-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21561228A>G , CM000663.2:g.21561228A>G	GRCh38
NC_000001.10:g.21887721A>G , CM000663.1:g.21887721A>G	GRCh37
NC_000001.9:g.21760308A>G	NCBI36
NG_008940.1:g.56864A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374840.8:c.297+16A>G MANE Select	ENSP00000363973.3:n.297+16A>G
ENST00000374832.5:c.297+16A>G	ENSP00000363965.1:n.297+16A>G
ENST00000374840.7:c.297+16A>G	ENSP00000363973.3:n.297+16A>G
ENST00000468526.1:n.357+16A>G
ENST00000539907.5:c.66+483A>G	ENSP00000437674.1:n.66+483A>G
ENST00000540617.5:c.132+16A>G	ENSP00000442672.1:n.132+16A>G
NM_000478.4:c.297+16A>G	NP_000469.3:n.297+16A>G
NM_001127501.2:c.132+16A>G	NP_001120973.2:n.132+16A>G
NM_001177520.1:c.66+483A>G	NP_001170991.1:n.66+483A>G
XM_005245818.1:c.297+16A>G	XP_005245875.1:n.297+16A>G
XM_005245820.2:c.297+16A>G	XP_005245877.1:n.297+16A>G
XM_006710546.1:c.297+16A>G	XP_006710609.1:n.297+16A>G
NM_000478.5:c.297+16A>G	NP_000469.3:n.297+16A>G
NM_001127501.3:c.132+16A>G	NP_001120973.2:n.132+16A>G
NM_001177520.2:c.66+483A>G	NP_001170991.1:n.66+483A>G
XM_006710546.3:c.297+16A>G	XP_006710609.1:n.297+16A>G
XM_017000903.1:c.141+16A>G	XP_016856392.1:n.141+16A>G
NM_000478.6:c.297+16A>G MANE Select	NP_000469.3:n.297+16A>G
NM_001127501.4:c.132+16A>G	NP_001120973.2:n.132+16A>G
NM_001177520.3:c.66+483A>G	NP_001170991.1:n.66+483A>G
NM_001369803.2:c.297+16A>G	NP_001356732.1:n.297+16A>G
NM_001369804.2:c.297+16A>G	NP_001356733.1:n.297+16A>G
NM_001369805.2:c.297+16A>G	NP_001356734.1:n.297+16A>G