Canonical Allele Identifier: CA1954662174
Gene: SOX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.16381982G= , CM000673.2:g.16381982G= GRCh38
NC_000011.9:g.16403528G= , CM000673.1:g.16403528G= GRCh37
NC_000011.8:g.16360104G= NCBI36
NG_012881.1:g.99408C=

Transcript Alleles

HGVS Amino-acid change
ENST00000527619.6:c.-5+20677C= ENSP00000434455.2:n.-5+20677C=
ENST00000655819.1:c.5+20677C= ENSP00000499737.1:n.5+20677C=
ENST00000396356.7:c.-4-40730C= ENSP00000379644.3:n.-4-40730C=
ENST00000526673.1:c.-5+306C= ENSP00000434892.1:n.-5+306C=
ENST00000527619.5:c.5+20677C= ENSP00000434455.1:n.5+20677C=
ENST00000528252.5:c.-5+26716C= ENSP00000432134.1:n.-5+26716C=
ENST00000528429.5:c.-5+20818C= ENSP00000433233.1:n.-5+20818C=
ENST00000529469.1:c.-4-40730C= ENSP00000432596.1:n.-4-40730C=
ENST00000530378.5:c.-4-40730C= ENSP00000432577.1:n.-4-40730C=
ENST00000533411.5:c.-5+15476C= ENSP00000436170.1:n.-5+15476C=
ENST00000533658.5:n.334-40730C=
NM_001145811.1:c.-5+26716C= NP_001139283.1:n.-5+26716C=
NM_001145819.1:c.35+20818C= NP_001139291.1:n.35+20818C=
NM_017508.2:c.5+20677C= NP_059978.1:n.5+20677C=
NM_033326.3:c.-4-40730C= NP_201583.2:n.-4-40730C=
NM_001145811.2:c.-5+26716C= NP_001139283.1:n.-5+26716C=
NM_001145819.2:c.-5+20818C= NP_001139291.2:n.-5+20818C=
NM_001367872.1:c.-4-40730C= NP_001354801.1:n.-4-40730C=
NM_017508.3:c.-5+20677C= NP_059978.2:n.-5+20677C=