Canonical Allele Identifier: CA390087454
Gene: SIX6 HGNC NCBI
C14orf39 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60509903C>A , CM000676.2:g.60509903C>A GRCh38
NC_000014.8:g.60976621C>A , CM000676.1:g.60976621C>A GRCh37
NC_000014.7:g.60046374C>A NCBI36
NG_008203.1:g.5684C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000327720.6:c.505C>A (SIX6) MANE Select ENSP00000328596.5:p.Pro169Thr
ENST00000327720.5:c.505C>A (SIX6) ENSP00000328596.5:p.Pro169Thr
ENST00000556799.1:c.-144+5492G>T (C14orf39) ENSP00000451441.1:n.-144+5492G>T
NM_007374.2:c.505C>A (SIX6) NP_031400.2:p.Pro169Thr
NM_007374.3:c.505C>A (SIX6) MANE Select NP_031400.2:p.Pro169Thr