Canonical Allele Identifier: CA1467351140

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745578_71745581delinsATAT , CM000666.2:g.71745578_71745581delinsATAT	GRCh38
NC_000004.11:g.72611295_72611298delinsATAT , CM000666.1:g.72611295_72611298delinsATAT	GRCh37
NC_000004.10:g.72830159_72830162delinsATAT	NCBI36
NG_012837.2:g.64940_64943delinsATAT
NG_012837.3:g.64940_64943delinsATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+570_*25+573delinsATAT MANE Select	ENSP00000273951.8:n.*25+570_*25+573delinsATAT
ENST00000273951.12:c.*25+570_*25+573delinsATAT	ENSP00000273951.8:n.*25+570_*25+573delinsATAT
ENST00000503364.5:n.123+570_123+573delinsATAT
ENST00000503472.5:n.1334+570_1334+573delinsATAT
ENST00000504199.5:c.*25+570_*25+573delinsATAT	ENSP00000421725.1:n.*25+570_*25+573delinsATAT
ENST00000509740.5:c.*273+570_*273+573delinsATAT	ENSP00000422664.1:n.*273+570_*273+573delinsATAT
ENST00000513476.5:c.1396-3711_1396-3708delinsATAT	ENSP00000426683.1:n.1396-3711_1396-3708delinsATAT
NM_000583.3:c.*25+570_*25+573delinsATAT	NP_000574.2:n.*25+570_*25+573delinsATAT
NM_001204306.1:c.*25+570_*25+573delinsATAT	NP_001191235.1:n.*25+570_*25+573delinsATAT
NM_001204307.1:c.*25+570_*25+573delinsATAT	NP_001191236.1:n.*25+570_*25+573delinsATAT
XM_006714177.2:c.*39+570_*39+573delinsATAT	XP_006714240.1:n.*39+570_*39+573delinsATAT
XM_006714177.3:c.*39+570_*39+573delinsATAT	XP_006714240.1:n.*39+570_*39+573delinsATAT
NM_000583.4:c.*25+570_*25+573delinsATAT MANE Select	NP_000574.2:n.*25+570_*25+573delinsATAT