Canonical Allele Identifier: CA1467351233

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745775_71745776delinsTC , CM000666.2:g.71745775_71745776delinsTC	GRCh38
NC_000004.11:g.72611492_72611493delinsTC , CM000666.1:g.72611492_72611493delinsTC	GRCh37
NC_000004.10:g.72830356_72830357delinsTC	NCBI36
NG_012837.2:g.64745_64746delinsGA
NG_012837.3:g.64745_64746delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+375_*25+376delinsGA MANE Select	ENSP00000273951.8:n.*25+375_*25+376delinsGA
ENST00000273951.12:c.*25+375_*25+376delinsGA	ENSP00000273951.8:n.*25+375_*25+376delinsGA
ENST00000503364.5:n.123+375_123+376delinsGA
ENST00000503472.5:n.1334+375_1334+376delinsGA
ENST00000504199.5:c.*25+375_*25+376delinsGA	ENSP00000421725.1:n.*25+375_*25+376delinsGA
ENST00000509740.5:c.*273+375_*273+376delinsGA	ENSP00000422664.1:n.*273+375_*273+376delinsGA
ENST00000513476.5:c.1396-3906_1396-3905delinsGA	ENSP00000426683.1:n.1396-3906_1396-3905delinsGA
NM_000583.3:c.*25+375_*25+376delinsGA	NP_000574.2:n.*25+375_*25+376delinsGA
NM_001204306.1:c.*25+375_*25+376delinsGA	NP_001191235.1:n.*25+375_*25+376delinsGA
NM_001204307.1:c.*25+375_*25+376delinsGA	NP_001191236.1:n.*25+375_*25+376delinsGA
XM_006714177.2:c.*39+375_*39+376delinsGA	XP_006714240.1:n.*39+375_*39+376delinsGA
XM_006714177.3:c.*39+375_*39+376delinsGA	XP_006714240.1:n.*39+375_*39+376delinsGA
NM_000583.4:c.*25+375_*25+376delinsGA MANE Select	NP_000574.2:n.*25+375_*25+376delinsGA