Canonical Allele Identifier: CA2706446304
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs2149290639

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71741882_71741883insACATGCTTCAGGACTACAGGATATTCT , CM000666.2:g.71741882_71741883insACATGCTTCAGGACTACAGGATATTCT GRCh38
NC_000004.11:g.72607599_72607600insACATGCTTCAGGACTACAGGATATTCT , CM000666.1:g.72607599_72607600insACATGCTTCAGGACTACAGGATATTCT GRCh37
NC_000004.10:g.72826463_72826464insACATGCTTCAGGACTACAGGATATTCT NCBI36
NG_012837.2:g.68638_68639insAGAATATCCTGTAGTCCTGAAGCATGT
NG_012837.3:g.68638_68639insAGAATATCCTGTAGTCCTGAAGCATGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.13:c.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT MANE Select ENSP00000273951.8:n.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCAT...
ENST00000273951.12:c.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT ENSP00000273951.8:n.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCAT...
ENST00000503364.5:n.124-13_124-12insAGAATATCCTGTAGTCCTGAAGCATGT
ENST00000503472.5:n.1335-13_1335-12insAGAATATCCTGTAGTCCTGAAGCATGT
ENST00000504199.5:c.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT ENSP00000421725.1:n.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCAT...
ENST00000509740.5:c.*274-13_*274-12insAGAATATCCTGTAGTCCTGAAGCATGT ENSP00000422664.1:n.*274-13_*274-12insAGAATATCCTGTAGTCCTGAAGC...
ENST00000513476.5:c.1396-13_1396-12insAGAATATCCTGTAGTCCTGAAGCATGT ENSP00000426683.1:n.1396-13_1396-12insAGAATATCCTGTAGTCCTGAAGC...
NM_000583.3:c.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT NP_000574.2:n.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT
NM_001204306.1:c.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT NP_001191235.1:n.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT
NM_001204307.1:c.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT NP_001191236.1:n.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT
XM_006714177.2:c.*40-13_*40-12insAGAATATCCTGTAGTCCTGAAGCATGT XP_006714240.1:n.*40-13_*40-12insAGAATATCCTGTAGTCCTGAAGCATGT
XM_006714177.3:c.*40-13_*40-12insAGAATATCCTGTAGTCCTGAAGCATGT XP_006714240.1:n.*40-13_*40-12insAGAATATCCTGTAGTCCTGAAGCATGT
NM_000583.4:c.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT MANE Select NP_000574.2:n.*26-13_*26-12insAGAATATCCTGTAGTCCTGAAGCATGT