Canonical Allele Identifier: CA385116258

Gene: HOXC9 HOXC6

Linked Data

• gnomAD v4: 12-54000715-A-T
• MyVariant Identifiers: chr12:g.54394499A>T (hg19) ; chr12:g.54000715A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000715A>T , CM000674.2:g.54000715A>T	GRCh38
NC_000012.11:g.54394499A>T , CM000674.1:g.54394499A>T	GRCh37
NC_000012.10:g.52680766A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303450.5:c.527A>T (HOXC9) MANE Select	ENSP00000302836.4:p.Asp176Val
ENST00000303450.4:c.527A>T (HOXC9)	ENSP00000302836.4:p.Asp176Val
ENST00000504315.1:c.-193+9901A>T (HOXC6)	ENSP00000424124.1:n.-193+9901A>T
ENST00000504557.1:n.123-1715A>T (HOXC9)
ENST00000508190.1:c.527A>T (HOXC9)	ENSP00000423861.1:p.Asp176Val
ENST00000509328.1:c.-73+5699A>T (HOXC6)	ENSP00000423898.1:n.-73+5699A>T
ENST00000513209.1:c.166+14705A>T	ENSP00000476742.1:n.166+14705A>T
NM_006897.1:c.527A>T (HOXC9)	NP_008828.1:p.Asp176Val
NM_006897.2:c.527A>T (HOXC9)	NP_008828.1:p.Asp176Val
NM_006897.3:c.527A>T (HOXC9) MANE Select	NP_008828.1:p.Asp176Val