Canonical Allele Identifier: CA507833837

Gene: SIX5

Linked Data

• MyVariant Identifiers: chr19:g.46270251C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45766993C>G , CM000681.2:g.45766993C>G	GRCh38
NC_000019.9:g.46270251C>G , CM000681.1:g.46270251C>G	GRCh37
NC_000019.8:g.50962091C>G	NCBI36
NG_012745.1:g.7247G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.966G>C MANE Select	ENSP00000316842.4:p.Leu322=
ENST00000317578.6:c.966G>C	ENSP00000316842.4:p.Leu322=
ENST00000560160.1:c.587-882G>C
ENST00000560168.1:c.*154G>C	ENSP00000453189.2:n.*154G>C
ENST00000622857.1:c.16-1031G>C	ENSP00000481365.1:n.16-1031G>C
NM_175875.4:c.966G>C	NP_787071.2:p.Leu322=
NM_175875.5:c.966G>C MANE Select	NP_787071.3:p.Leu322=