Canonical Allele Identifier: CA2037230498

Gene: HOXC9 HOXC6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000623G= , CM000674.2:g.54000623G=	GRCh38
NC_000012.11:g.54394407G= , CM000674.1:g.54394407G=	GRCh37
NC_000012.10:g.52680674G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303450.5:c.435G= (HOXC9) MANE Select	ENSP00000302836.4:p.Ser145=
ENST00000303450.4:c.435G= (HOXC9)	ENSP00000302836.4:p.Ser145=
ENST00000504315.1:c.-193+9809G= (HOXC6)	ENSP00000424124.1:n.-193+9809G=
ENST00000504557.1:n.123-1807G= (HOXC9)
ENST00000508190.1:c.435G= (HOXC9)	ENSP00000423861.1:p.Ser145=
ENST00000509328.1:c.-73+5607G= (HOXC6)	ENSP00000423898.1:n.-73+5607G=
ENST00000513209.1:c.166+14613G=	ENSP00000476742.1:n.166+14613G=
NM_006897.1:c.435G= (HOXC9)	NP_008828.1:p.Ser145=
NM_006897.2:c.435G= (HOXC9)	NP_008828.1:p.Ser145=
NM_006897.3:c.435G= (HOXC9) MANE Select	NP_008828.1:p.Ser145=