Canonical Allele Identifier: CA2643931728

Gene: ALPL

Linked Data

• gnomAD v4: 1-21575932-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.21575932G>A , CM000663.2:g.21575932G>A	GRCh38
NC_000001.10:g.21902425G>A , CM000663.1:g.21902425G>A	GRCh37
NC_000001.9:g.21775012G>A	NCBI36
NG_008940.1:g.71568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374840.8:c.1189+8G>A MANE Select	ENSP00000363973.3:n.1189+8G>A
ENST00000374829.2:n.458+8G>A
ENST00000374830.2:c.264+8G>A
ENST00000374832.5:c.1189+8G>A	ENSP00000363965.1:n.1189+8G>A
ENST00000374840.7:c.1189+8G>A	ENSP00000363973.3:n.1189+8G>A
ENST00000539907.5:c.958+8G>A	ENSP00000437674.1:n.958+8G>A
ENST00000540617.5:c.1024+8G>A	ENSP00000442672.1:n.1024+8G>A
NM_000478.4:c.1189+8G>A	NP_000469.3:n.1189+8G>A
NM_001127501.2:c.1024+8G>A	NP_001120973.2:n.1024+8G>A
NM_001177520.1:c.958+8G>A	NP_001170991.1:n.958+8G>A
XM_005245818.1:c.1189+8G>A	XP_005245875.1:n.1189+8G>A
XM_006710546.1:c.1189+8G>A	XP_006710609.1:n.1189+8G>A
NM_000478.5:c.1189+8G>A	NP_000469.3:n.1189+8G>A
NM_001127501.3:c.1024+8G>A	NP_001120973.2:n.1024+8G>A
NM_001177520.2:c.958+8G>A	NP_001170991.1:n.958+8G>A
XM_006710546.3:c.1189+8G>A	XP_006710609.1:n.1189+8G>A
XM_017000903.1:c.1033+8G>A	XP_016856392.1:n.1033+8G>A
NM_000478.6:c.1189+8G>A MANE Select	NP_000469.3:n.1189+8G>A
NM_001127501.4:c.1024+8G>A	NP_001120973.2:n.1024+8G>A
NM_001177520.3:c.958+8G>A	NP_001170991.1:n.958+8G>A
NM_001369803.2:c.1189+8G>A	NP_001356732.1:n.1189+8G>A
NM_001369804.2:c.1189+8G>A	NP_001356733.1:n.1189+8G>A
NM_001369805.2:c.1189+8G>A	NP_001356734.1:n.1189+8G>A