Canonical Allele Identifier: CA2575582719
Gene: SIX6 HGNC NCBI
C14orf39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60509904dup , CM000676.2:g.60509904dup GRCh38
NC_000014.8:g.60976622dup , CM000676.1:g.60976622dup GRCh37
NC_000014.7:g.60046375dup NCBI36
NG_008203.1:g.5685dup

Transcript Alleles

HGVS Amino-acid change
ENST00000327720.6:c.506dup (SIX6) MANE Select ENSP00000328596.5:p.Thr170TyrfsTer?
ENST00000327720.5:c.506dup (SIX6) ENSP00000328596.5:p.Thr170TyrfsTer?
ENST00000556799.1:c.-144+5494dup (C14orf39) ENSP00000451441.1:n.-144+5494dup
NM_007374.2:c.506dup (SIX6) NP_031400.2:p.Thr170TyrfsTer?
NM_007374.3:c.506dup (SIX6) MANE Select NP_031400.2:p.Thr170TyrfsTer?