Canonical Allele Identifier: CA2706446224
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs2149290637

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71741881_71741882insTTCTTCAATTCAGC , CM000666.2:g.71741881_71741882insTTCTTCAATTCAGC GRCh38
NC_000004.11:g.72607598_72607599insTTCTTCAATTCAGC , CM000666.1:g.72607598_72607599insTTCTTCAATTCAGC GRCh37
NC_000004.10:g.72826462_72826463insTTCTTCAATTCAGC NCBI36
NG_012837.2:g.68639_68640insGCTGAATTGAAGAA
NG_012837.3:g.68639_68640insGCTGAATTGAAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.13:c.*26-12_*26-11insGCTGAATTGAAGAA MANE Select ENSP00000273951.8:n.*26-12_*26-11insGCTGAATTGAAGAA
ENST00000273951.12:c.*26-12_*26-11insGCTGAATTGAAGAA ENSP00000273951.8:n.*26-12_*26-11insGCTGAATTGAAGAA
ENST00000503364.5:n.124-12_124-11insGCTGAATTGAAGAA
ENST00000503472.5:n.1335-12_1335-11insGCTGAATTGAAGAA
ENST00000504199.5:c.*26-12_*26-11insGCTGAATTGAAGAA ENSP00000421725.1:n.*26-12_*26-11insGCTGAATTGAAGAA
ENST00000509740.5:c.*274-12_*274-11insGCTGAATTGAAGAA ENSP00000422664.1:n.*274-12_*274-11insGCTGAATTGAAGAA
ENST00000513476.5:c.1396-12_1396-11insGCTGAATTGAAGAA ENSP00000426683.1:n.1396-12_1396-11insGCTGAATTGAAGAA
NM_000583.3:c.*26-12_*26-11insGCTGAATTGAAGAA NP_000574.2:n.*26-12_*26-11insGCTGAATTGAAGAA
NM_001204306.1:c.*26-12_*26-11insGCTGAATTGAAGAA NP_001191235.1:n.*26-12_*26-11insGCTGAATTGAAGAA
NM_001204307.1:c.*26-12_*26-11insGCTGAATTGAAGAA NP_001191236.1:n.*26-12_*26-11insGCTGAATTGAAGAA
XM_006714177.2:c.*40-12_*40-11insGCTGAATTGAAGAA XP_006714240.1:n.*40-12_*40-11insGCTGAATTGAAGAA
XM_006714177.3:c.*40-12_*40-11insGCTGAATTGAAGAA XP_006714240.1:n.*40-12_*40-11insGCTGAATTGAAGAA
NM_000583.4:c.*26-12_*26-11insGCTGAATTGAAGAA MANE Select NP_000574.2:n.*26-12_*26-11insGCTGAATTGAAGAA