Canonical Allele Identifier: CA2706446147
Gene: GC HGNC NCBI

Linked Data

dbSNP Id: rs2149290627

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71741875_71741876insCTTCAGGACTAC , CM000666.2:g.71741875_71741876insCTTCAGGACTAC GRCh38
NC_000004.11:g.72607592_72607593insCTTCAGGACTAC , CM000666.1:g.72607592_72607593insCTTCAGGACTAC GRCh37
NC_000004.10:g.72826456_72826457insCTTCAGGACTAC NCBI36
NG_012837.2:g.68645_68646insGTAGTCCTGAAG
NG_012837.3:g.68645_68646insGTAGTCCTGAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.13:c.*26-6_*26-5insGTAGTCCTGAAG MANE Select ENSP00000273951.8:n.*26-6_*26-5insGTAGTCCTGAAG
ENST00000273951.12:c.*26-6_*26-5insGTAGTCCTGAAG ENSP00000273951.8:n.*26-6_*26-5insGTAGTCCTGAAG
ENST00000503364.5:n.124-6_124-5insGTAGTCCTGAAG
ENST00000503472.5:n.1335-6_1335-5insGTAGTCCTGAAG
ENST00000504199.5:c.*26-6_*26-5insGTAGTCCTGAAG ENSP00000421725.1:n.*26-6_*26-5insGTAGTCCTGAAG
ENST00000509740.5:c.*274-6_*274-5insGTAGTCCTGAAG ENSP00000422664.1:n.*274-6_*274-5insGTAGTCCTGAAG
ENST00000513476.5:c.1396-6_1396-5insGTAGTCCTGAAG ENSP00000426683.1:n.1396-6_1396-5insGTAGTCCTGAAG
NM_000583.3:c.*26-6_*26-5insGTAGTCCTGAAG NP_000574.2:n.*26-6_*26-5insGTAGTCCTGAAG
NM_001204306.1:c.*26-6_*26-5insGTAGTCCTGAAG NP_001191235.1:n.*26-6_*26-5insGTAGTCCTGAAG
NM_001204307.1:c.*26-6_*26-5insGTAGTCCTGAAG NP_001191236.1:n.*26-6_*26-5insGTAGTCCTGAAG
XM_006714177.2:c.*40-6_*40-5insGTAGTCCTGAAG XP_006714240.1:n.*40-6_*40-5insGTAGTCCTGAAG
XM_006714177.3:c.*40-6_*40-5insGTAGTCCTGAAG XP_006714240.1:n.*40-6_*40-5insGTAGTCCTGAAG
NM_000583.4:c.*26-6_*26-5insGTAGTCCTGAAG MANE Select NP_000574.2:n.*26-6_*26-5insGTAGTCCTGAAG