Canonical Allele Identifier: CA406419639
Gene: SIX5 HGNC NCBI

Linked Data

dbSNP Id: rs1344313680

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766886G>C , CM000681.2:g.45766886G>C GRCh38
NC_000019.9:g.46270144G>C , CM000681.1:g.46270144G>C GRCh37
NC_000019.8:g.50961984G>C NCBI36
NG_012745.1:g.7354C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1073C>G MANE Select ENSP00000316842.4:p.Pro358Arg
ENST00000317578.6:c.1073C>G ENSP00000316842.4:p.Pro358Arg
ENST00000560160.1:c.587-775C>G
ENST00000560168.1:c.*261C>G ENSP00000453189.2:n.*261C>G
ENST00000622857.1:c.16-924C>G ENSP00000481365.1:n.16-924C>G
NM_175875.4:c.1073C>G NP_787071.2:p.Pro358Arg
NM_175875.5:c.1073C>G MANE Select NP_787071.3:p.Pro358Arg