Canonical Allele Identifier: CA2619103745

Gene: HOXC9 HOXC6

Linked Data

• gnomAD v4: 12-54000713-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000713_54000714insT , CM000674.2:g.54000713_54000714insT	GRCh38
NC_000012.11:g.54394497_54394498insT , CM000674.1:g.54394497_54394498insT	GRCh37
NC_000012.10:g.52680764_52680765insT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303450.5:c.525_526insT (HOXC9) MANE Select	ENSP00000302836.4:p.Asp176Ter
ENST00000303450.4:c.525_526insT (HOXC9)	ENSP00000302836.4:p.Asp176Ter
ENST00000504315.1:c.-193+9899_-193+9900insT (HOXC6)	ENSP00000424124.1:n.-193+9899_-193+9900insT
ENST00000504557.1:n.123-1717_123-1716insT (HOXC9)
ENST00000508190.1:c.525_526insT (HOXC9)	ENSP00000423861.1:p.Asp176Ter
ENST00000509328.1:c.-73+5697_-73+5698insT (HOXC6)	ENSP00000423898.1:n.-73+5697_-73+5698insT
ENST00000513209.1:c.166+14703_166+14704insT	ENSP00000476742.1:n.166+14703_166+14704insT
NM_006897.1:c.525_526insT (HOXC9)	NP_008828.1:p.Asp176Ter
NM_006897.2:c.525_526insT (HOXC9)	NP_008828.1:p.Asp176Ter
NM_006897.3:c.525_526insT (HOXC9) MANE Select	NP_008828.1:p.Asp176Ter