Canonical Allele Identifier: CA2517232800

Gene: HLA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269482_31269483insTCCCTTGTCCCGCTTCCTTGCCCTTCTCTGCTCTCTCAAATCCTCATCAGTCATCATCAATCACCCCCCTCTCTCATCTCTCCCCTGACCCCTCACCTACCCTCTGCAC , CM000668.2:g.31269482_31269483insTCCCTTGTCCCGCTTCCTTGCCCTTCTCTGCTCTCTCAAATCCTCATCAGTCATCATCAATCACCCCCCTCTCTCATCTCTCCCCTGACCCCTCACCTACCCTCTGCAC	GRCh38
NC_000006.11:g.31237259_31237260insTCCCTTGTCCCGCTTCCTTGCCCTTCTCTGCTCTCTCAAATCCTCATCAGTCATCATCAATCACCCCCCTCTCTCATCTCTCCCCTGACCCCTCACCTACCCTCTGCAC , CM000668.1:g.31237259_31237260insTCCCTTGTCCCGCTTCCTTGCCCTTCTCTGCTCTCTCAAATCCTCATCAGTCATCATCAATCACCCCCCTCTCTCATCTCTCCCCTGACCCCTCACCTACCCTCTGCAC	GRCh37
NC_000006.10:g.31345238_31345239insTCCCTTGTCCCGCTTCCTTGCCCTTCTCTGCTCTCTCAAATCCTCATCAGTCATCATCAATCACCCCCCTCTCTCATCTCTCCCCTGACCCCTCACCTACCCTCTGCAC	NCBI36
NG_029422.2:g.7650_7651insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG MANE Select	ENSP00000365402.5:n.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCA...
ENST00000376228.9:c.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG	ENSP00000365402.5:n.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCA...
ENST00000376237.8:c.*635+11_*635+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG	ENSP00000365412.4:n.*635+11_*635+12insTGCAGAGGGTAGGTGAGGGGTCA...
ENST00000383329.7:c.1066+11_1066+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG	ENSP00000372819.3:n.1066+11_1066+12insTGCAGAGGGTAGGTGAGGGGTCA...
ENST00000466892.5:n.185_186insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG
ENST00000470363.5:n.806+11_806+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG
ENST00000487245.5:n.1407+11_1407+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG
NM_002117.5:c.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG	NP_002108.4:n.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAG...
NM_002117.6:c.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAGAGATGAGAGAGGGGGGTGATTGATGATGACTGATGAGGATTTGAGAGAGCAGAGAAGGGCAAGGAAGCGGGACAAGGGAG MANE Select	NP_002108.4:n.1048+11_1048+12insTGCAGAGGGTAGGTGAGGGGTCAGGGGAG...