Canonical Allele Identifier: CA419401483

Linked Data

MyVariant Identifiers: chr1:g.110607212T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064590T>A , CM000663.2:g.110064590T>A GRCh38
NC_000001.10:g.110607212T>A , CM000663.1:g.110607212T>A GRCh37
NC_000001.9:g.110408735T>A NCBI36
NG_012039.1:g.11111A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.591A>T (ALX3) MANE Select ENSP00000497310.1:p.Val197=
ENST00000649954.1:c.162A>T (ALX3) ENSP00000497035.1:p.Val54=
ENST00000369792.4:c.591A>T (ALX3) ENSP00000358807.3:p.Val197=
ENST00000473429.5:n.4214-7865T>A (STRIP1)
NM_006492.2:c.591A>T (ALX3) NP_006483.2:p.Val197=
NM_006492.3:c.591A>T (ALX3) MANE Select NP_006483.2:p.Val197=