Canonical Allele Identifier: CA2762138125

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741873_71741874insATAAACATGCTTCAGGACTACAGGATATTCTTCAATTCAGCATCAATCTCTGAATCACAGTAAAGAGGAGG , CM000666.2:g.71741873_71741874insATAAACATGCTTCAGGACTACAGGATATTCTTCAATTCAGCATCAATCTCTGAATCACAGTAAAGAGGAGG	GRCh38
NC_000004.11:g.72607590_72607591insATAAACATGCTTCAGGACTACAGGATATTCTTCAATTCAGCATCAATCTCTGAATCACAGTAAAGAGGAGG , CM000666.1:g.72607590_72607591insATAAACATGCTTCAGGACTACAGGATATTCTTCAATTCAGCATCAATCTCTGAATCACAGTAAAGAGGAGG	GRCh37
NC_000004.10:g.72826454_72826455insATAAACATGCTTCAGGACTACAGGATATTCTTCAATTCAGCATCAATCTCTGAATCACAGTAAAGAGGAGG	NCBI36
NG_012837.2:g.68647_68648insCCTCCTCTTTACTGTGATTCAGAGATTGATGCTGAATTGAAGAATATCCTGTAGTCCTGAAGCATGTTTAT
NG_012837.3:g.68647_68648insCCTCCTCTTTACTGTGATTCAGAGATTGATGCTGAATTGAAGAATATCCTGTAGTCCTGAAGCATGTTTAT

Transcript Alleles

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