Canonical Allele Identifier: CA525315859

Gene: ALX3 STRIP1

Linked Data

• dbSNP Id: rs1270646277
• gnomAD v2: 1-110607174-G-T
• gnomAD v4: 1-110064552-G-T
• MyVariant Identifiers: chr1:g.110607174G>T (hg19) ; chr1:g.110064552G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110064552G>T , CM000663.2:g.110064552G>T	GRCh38
NC_000001.10:g.110607174G>T , CM000663.1:g.110607174G>T	GRCh37
NC_000001.9:g.110408697G>T	NCBI36
NG_012039.1:g.11149C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647563.2:c.594+35C>A (ALX3) MANE Select	ENSP00000497310.1:n.594+35C>A
ENST00000649954.1:c.165+35C>A (ALX3)	ENSP00000497035.1:n.165+35C>A
ENST00000369792.4:c.594+35C>A (ALX3)	ENSP00000358807.3:n.594+35C>A
ENST00000473429.5:n.4214-7903G>T (STRIP1)
NM_006492.2:c.594+35C>A (ALX3)	NP_006483.2:n.594+35C>A
NM_006492.3:c.594+35C>A (ALX3) MANE Select	NP_006483.2:n.594+35C>A