Canonical Allele Identifier: CA2037230552

Gene: HOXC9 HOXC6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000717C= , CM000674.2:g.54000717C=	GRCh38
NC_000012.11:g.54394501C= , CM000674.1:g.54394501C=	GRCh37
NC_000012.10:g.52680768C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000303450.5:c.529C= (HOXC9) MANE Select	ENSP00000302836.4:p.Leu177=
ENST00000303450.4:c.529C= (HOXC9)	ENSP00000302836.4:p.Leu177=
ENST00000504315.1:c.-193+9903C= (HOXC6)	ENSP00000424124.1:n.-193+9903C=
ENST00000504557.1:n.123-1713C= (HOXC9)
ENST00000508190.1:c.529C= (HOXC9)	ENSP00000423861.1:p.Leu177=
ENST00000509328.1:c.-73+5701C= (HOXC6)	ENSP00000423898.1:n.-73+5701C=
ENST00000513209.1:c.166+14707C=	ENSP00000476742.1:n.166+14707C=
NM_006897.1:c.529C= (HOXC9)	NP_008828.1:p.Leu177=
NM_006897.2:c.529C= (HOXC9)	NP_008828.1:p.Leu177=
NM_006897.3:c.529C= (HOXC9) MANE Select	NP_008828.1:p.Leu177=