Canonical Allele Identifier: CA2037230553

Gene: HOXC9 HOXC6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000718T= , CM000674.2:g.54000718T=	GRCh38
NC_000012.11:g.54394502T= , CM000674.1:g.54394502T=	GRCh37
NC_000012.10:g.52680769T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303450.5:c.530T= (HOXC9) MANE Select	ENSP00000302836.4:p.Leu177=
ENST00000303450.4:c.530T= (HOXC9)	ENSP00000302836.4:p.Leu177=
ENST00000504315.1:c.-193+9904T= (HOXC6)	ENSP00000424124.1:n.-193+9904T=
ENST00000504557.1:n.123-1712T= (HOXC9)
ENST00000508190.1:c.530T= (HOXC9)	ENSP00000423861.1:p.Leu177=
ENST00000509328.1:c.-73+5702T= (HOXC6)	ENSP00000423898.1:n.-73+5702T=
ENST00000513209.1:c.166+14708T=	ENSP00000476742.1:n.166+14708T=
NM_006897.1:c.530T= (HOXC9)	NP_008828.1:p.Leu177=
NM_006897.2:c.530T= (HOXC9)	NP_008828.1:p.Leu177=
NM_006897.3:c.530T= (HOXC9) MANE Select	NP_008828.1:p.Leu177=