Canonical Allele Identifier: CA480091581

Gene: HOXC9 HOXC6

Linked Data

• dbSNP Id: rs932151797
• gnomAD v2: 12-54394501-C-T
• gnomAD v4: 12-54000717-C-T
• MyVariant Identifiers: chr12:g.54394501C>T (hg19) ; chr12:g.54000717C>T (hg38)

Genomic Alleles

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

Transcript Alleles

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