Canonical Allele Identifier: CA2140829101

Gene: SIX6 C14orf39

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.60509901C= , CM000676.2:g.60509901C=	GRCh38
NC_000014.8:g.60976619C= , CM000676.1:g.60976619C=	GRCh37
NC_000014.7:g.60046372C=	NCBI36
NG_008203.1:g.5682C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000327720.6:c.503C= (SIX6) MANE Select	ENSP00000328596.5:p.Thr168=
ENST00000327720.5:c.503C= (SIX6)	ENSP00000328596.5:p.Thr168=
ENST00000556799.1:c.-144+5494G= (C14orf39)	ENSP00000451441.1:n.-144+5494G=
NM_007374.2:c.503C= (SIX6)	NP_031400.2:p.Thr168=
NM_007374.3:c.503C= (SIX6) MANE Select	NP_031400.2:p.Thr168=