Canonical Allele Identifier: CA947811309

Gene: HOXC9 HOXC6

Linked Data

• dbSNP Id: rs1939724309
• gnomAD v3: 12-54000799-ACAGCCCTCCCGAACCGTG-A
• gnomAD v4: 12-54000799-ACAGCCCTCCCGAACCGTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.54000803_54000820del , CM000674.2:g.54000803_54000820del	GRCh38
NC_000012.11:g.54394587_54394604del , CM000674.1:g.54394587_54394604del	GRCh37
NC_000012.10:g.52680854_52680871del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303450.5:c.538+77_538+94del (HOXC9) MANE Select	ENSP00000302836.4:n.538+77_538+94del
ENST00000303450.4:c.538+77_538+94del (HOXC9)	ENSP00000302836.4:n.538+77_538+94del
ENST00000504315.1:c.-193+9989_-193+10006del (HOXC6)	ENSP00000424124.1:n.-193+9989_-193+10006del
ENST00000504557.1:n.123-1627_123-1610del (HOXC9)
ENST00000508190.1:c.538+77_538+94del (HOXC9)	ENSP00000423861.1:n.538+77_538+94del
ENST00000509328.1:c.-73+5787_-73+5804del (HOXC6)	ENSP00000423898.1:n.-73+5787_-73+5804del
ENST00000513209.1:c.166+14793_166+14810del	ENSP00000476742.1:n.166+14793_166+14810del
NM_006897.1:c.538+77_538+94del (HOXC9)	NP_008828.1:n.538+77_538+94del
NM_006897.2:c.538+77_538+94del (HOXC9)	NP_008828.1:n.538+77_538+94del
NM_006897.3:c.538+77_538+94del (HOXC9) MANE Select	NP_008828.1:n.538+77_538+94del