Canonical Allele Identifier: CA390087441
Gene: SIX6 HGNC NCBI
C14orf39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60509898T>C , CM000676.2:g.60509898T>C GRCh38
NC_000014.8:g.60976616T>C , CM000676.1:g.60976616T>C GRCh37
NC_000014.7:g.60046369T>C NCBI36
NG_008203.1:g.5679T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327720.6:c.500T>C (SIX6) MANE Select ENSP00000328596.5:p.Leu167Pro
ENST00000327720.5:c.500T>C (SIX6) ENSP00000328596.5:p.Leu167Pro
ENST00000556799.1:c.-144+5497A>G (C14orf39) ENSP00000451441.1:n.-144+5497A>G
NM_007374.2:c.500T>C (SIX6) NP_031400.2:p.Leu167Pro
NM_007374.3:c.500T>C (SIX6) MANE Select NP_031400.2:p.Leu167Pro