Canonical Allele Identifier: CA419401482

Linked Data

MyVariant Identifiers: chr1:g.110607209C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110064587C>T , CM000663.2:g.110064587C>T GRCh38
NC_000001.10:g.110607209C>T , CM000663.1:g.110607209C>T GRCh37
NC_000001.9:g.110408732C>T NCBI36
NG_012039.1:g.11114G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000647563.2:c.594G>A (ALX3) MANE Select ENSP00000497310.1:p.Gln198=
ENST00000649954.1:c.165G>A (ALX3) ENSP00000497035.1:p.Gln55=
ENST00000369792.4:c.594G>A (ALX3) ENSP00000358807.3:p.Gln198=
ENST00000473429.5:n.4214-7868C>T (STRIP1)
NM_006492.2:c.594G>A (ALX3) NP_006483.2:p.Gln198=
NM_006492.3:c.594G>A (ALX3) MANE Select NP_006483.2:p.Gln198=