Canonical Allele Identifier: CA2140828866
Gene: SIX6 HGNC NCBI
C14orf39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60509835G= , CM000676.2:g.60509835G= GRCh38
NC_000014.8:g.60976553G= , CM000676.1:g.60976553G= GRCh37
NC_000014.7:g.60046306G= NCBI36
NG_008203.1:g.5616G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000327720.6:c.437G= (SIX6) MANE Select ENSP00000328596.5:p.Trp146=
ENST00000327720.5:c.437G= (SIX6) ENSP00000328596.5:p.Trp146=
ENST00000556799.1:c.-144+5560C= (C14orf39) ENSP00000451441.1:n.-144+5560C=
NM_007374.2:c.437G= (SIX6) NP_031400.2:p.Trp146=
NM_007374.3:c.437G= (SIX6) MANE Select NP_031400.2:p.Trp146=
Search 100 bp 5'
Search 100 bp 3'