Canonical Allele Identifier: CA2037230576

Linked Data

dbSNP Id: rs770065757

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.54000768_54000777del , CM000674.2:g.54000768_54000777del GRCh38
NC_000012.11:g.54394552_54394561del , CM000674.1:g.54394552_54394561del GRCh37
NC_000012.10:g.52680819_52680828del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000303450.5:c.538+42_538+51del (HOXC9) MANE Select ENSP00000302836.4:n.538+42_538+51del
ENST00000303450.4:c.538+42_538+51del (HOXC9) ENSP00000302836.4:n.538+42_538+51del
ENST00000504315.1:c.-193+9954_-193+9963del (HOXC6) ENSP00000424124.1:n.-193+9954_-193+9963del
ENST00000504557.1:n.123-1662_123-1653del (HOXC9)
ENST00000508190.1:c.538+42_538+51del (HOXC9) ENSP00000423861.1:n.538+42_538+51del
ENST00000509328.1:c.-73+5752_-73+5761del (HOXC6) ENSP00000423898.1:n.-73+5752_-73+5761del
ENST00000513209.1:c.166+14758_166+14767del ENSP00000476742.1:n.166+14758_166+14767del
NM_006897.1:c.538+42_538+51del (HOXC9) NP_008828.1:n.538+42_538+51del
NM_006897.2:c.538+42_538+51del (HOXC9) NP_008828.1:n.538+42_538+51del
NM_006897.3:c.538+42_538+51del (HOXC9) MANE Select NP_008828.1:n.538+42_538+51del