Canonical Allele Identifier: CA2619104238

Gene: HOXC9 HOXC6

Linked Data

• gnomAD v4: 12-54000807-CCCGAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000811_54000815del , CM000674.2:g.54000811_54000815del	GRCh38
NC_000012.11:g.54394595_54394599del , CM000674.1:g.54394595_54394599del	GRCh37
NC_000012.10:g.52680862_52680866del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303450.5:c.538+85_538+89del (HOXC9) MANE Select	ENSP00000302836.4:n.538+85_538+89del
ENST00000303450.4:c.538+85_538+89del (HOXC9)	ENSP00000302836.4:n.538+85_538+89del
ENST00000504315.1:c.-193+9997_-193+10001del (HOXC6)	ENSP00000424124.1:n.-193+9997_-193+10001del
ENST00000504557.1:n.123-1619_123-1615del (HOXC9)
ENST00000508190.1:c.538+85_538+89del (HOXC9)	ENSP00000423861.1:n.538+85_538+89del
ENST00000509328.1:c.-73+5795_-73+5799del (HOXC6)	ENSP00000423898.1:n.-73+5795_-73+5799del
ENST00000513209.1:c.166+14801_166+14805del	ENSP00000476742.1:n.166+14801_166+14805del
NM_006897.1:c.538+85_538+89del (HOXC9)	NP_008828.1:n.538+85_538+89del
NM_006897.2:c.538+85_538+89del (HOXC9)	NP_008828.1:n.538+85_538+89del
NM_006897.3:c.538+85_538+89del (HOXC9) MANE Select	NP_008828.1:n.538+85_538+89del