Canonical Allele Identifier: CA1467372834

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755940_71755944delinsCTATT , CM000666.2:g.71755940_71755944delinsCTATT	GRCh38
NC_000004.11:g.72621657_72621661delinsCTATT , CM000666.1:g.72621657_72621661delinsCTATT	GRCh37
NC_000004.10:g.72840521_72840525delinsCTATT	NCBI36
NG_012837.2:g.54577_54581delinsAATAG
NG_012837.3:g.54577_54581delinsAATAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1034+768_1034+772delinsAATAG MANE Select	ENSP00000273951.8:n.1034+768_1034+772delinsAATAG
ENST00000273951.12:c.1034+768_1034+772delinsAATAG	ENSP00000273951.8:n.1034+768_1034+772delinsAATAG
ENST00000503472.5:n.918+768_918+772delinsAATAG
ENST00000504199.5:c.1091+768_1091+772delinsAATAG	ENSP00000421725.1:n.1091+768_1091+772delinsAATAG
ENST00000509740.5:c.1034+768_1034+772delinsAATAG	ENSP00000422664.1:n.1034+768_1034+772delinsAATAG
ENST00000513476.5:c.1034+768_1034+772delinsAATAG	ENSP00000426683.1:n.1034+768_1034+772delinsAATAG
NM_000583.3:c.1034+768_1034+772delinsAATAG	NP_000574.2:n.1034+768_1034+772delinsAATAG
NM_001204306.1:c.1034+768_1034+772delinsAATAG	NP_001191235.1:n.1034+768_1034+772delinsAATAG
NM_001204307.1:c.1091+768_1091+772delinsAATAG	NP_001191236.1:n.1091+768_1091+772delinsAATAG
XM_006714177.2:c.1034+768_1034+772delinsAATAG	XP_006714240.1:n.1034+768_1034+772delinsAATAG
XM_006714177.3:c.1034+768_1034+772delinsAATAG	XP_006714240.1:n.1034+768_1034+772delinsAATAG
NM_000583.4:c.1034+768_1034+772delinsAATAG MANE Select	NP_000574.2:n.1034+768_1034+772delinsAATAG