Canonical Allele Identifier: CA390087435
Gene: SIX6 HGNC NCBI
C14orf39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60509895G>C , CM000676.2:g.60509895G>C GRCh38
NC_000014.8:g.60976613G>C , CM000676.1:g.60976613G>C GRCh37
NC_000014.7:g.60046366G>C NCBI36
NG_008203.1:g.5676G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327720.6:c.497G>C (SIX6) MANE Select ENSP00000328596.5:p.Gly166Ala
ENST00000327720.5:c.497G>C (SIX6) ENSP00000328596.5:p.Gly166Ala
ENST00000556799.1:c.-144+5500C>G (C14orf39) ENSP00000451441.1:n.-144+5500C>G
NM_007374.2:c.497G>C (SIX6) NP_031400.2:p.Gly166Ala
NM_007374.3:c.497G>C (SIX6) MANE Select NP_031400.2:p.Gly166Ala