Canonical Allele Identifier: CA1467380570

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71772990_71772994delinsCTAAT , CM000666.2:g.71772990_71772994delinsCTAAT	GRCh38
NC_000004.11:g.72638707_72638711delinsCTAAT , CM000666.1:g.72638707_72638711delinsCTAAT	GRCh37
NC_000004.10:g.72857571_72857575delinsCTAAT	NCBI36
NG_012837.2:g.37527_37531delinsATTAG
NG_012837.3:g.37527_37531delinsATTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.59-3594_59-3590delinsATTAG MANE Select	ENSP00000273951.8:n.59-3594_59-3590delinsATTAG
ENST00000273951.12:c.59-3594_59-3590delinsATTAG	ENSP00000273951.8:n.59-3594_59-3590delinsATTAG
ENST00000504199.5:c.116-3594_116-3590delinsATTAG	ENSP00000421725.1:n.116-3594_116-3590delinsATTAG
ENST00000506245.1:c.59-3594_59-3590delinsATTAG	ENSP00000426718.1:n.59-3594_59-3590delinsATTAG
ENST00000509740.5:c.59-3594_59-3590delinsATTAG	ENSP00000422664.1:n.59-3594_59-3590delinsATTAG
ENST00000513476.5:c.59-3594_59-3590delinsATTAG	ENSP00000426683.1:n.59-3594_59-3590delinsATTAG
NM_000583.3:c.59-3594_59-3590delinsATTAG	NP_000574.2:n.59-3594_59-3590delinsATTAG
NM_001204306.1:c.59-3594_59-3590delinsATTAG	NP_001191235.1:n.59-3594_59-3590delinsATTAG
NM_001204307.1:c.116-3594_116-3590delinsATTAG	NP_001191236.1:n.116-3594_116-3590delinsATTAG
XM_006714177.2:c.59-3594_59-3590delinsATTAG	XP_006714240.1:n.59-3594_59-3590delinsATTAG
XM_006714177.3:c.59-3594_59-3590delinsATTAG	XP_006714240.1:n.59-3594_59-3590delinsATTAG
NM_000583.4:c.59-3594_59-3590delinsATTAG MANE Select	NP_000574.2:n.59-3594_59-3590delinsATTAG