Canonical Allele Identifier: CA798103398

Gene: GC

Linked Data

• dbSNP Id: rs1388852703
• gnomAD v3: 4-71745580-ATTG-A
• gnomAD v4: 4-71745580-ATTG-A
• MyVariant Identifiers: chr4:g.72611298_72611300del (hg19) ; chr4:g.71745581_71745583del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71745587_71745589del , CM000666.2:g.71745587_71745589del	GRCh38
NC_000004.11:g.72611304_72611306del , CM000666.1:g.72611304_72611306del	GRCh37
NC_000004.10:g.72830168_72830170del	NCBI36
NG_012837.2:g.64938_64940del
NG_012837.3:g.64938_64940del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*25+568_*25+570del MANE Select	ENSP00000273951.8:n.*25+568_*25+570del
ENST00000273951.12:c.*25+568_*25+570del	ENSP00000273951.8:n.*25+568_*25+570del
ENST00000503364.5:n.123+568_123+570del
ENST00000503472.5:n.1334+568_1334+570del
ENST00000504199.5:c.*25+568_*25+570del	ENSP00000421725.1:n.*25+568_*25+570del
ENST00000509740.5:c.*273+568_*273+570del	ENSP00000422664.1:n.*273+568_*273+570del
ENST00000513476.5:c.1396-3713_1396-3711del	ENSP00000426683.1:n.1396-3713_1396-3711del
NM_000583.3:c.*25+568_*25+570del	NP_000574.2:n.*25+568_*25+570del
NM_001204306.1:c.*25+568_*25+570del	NP_001191235.1:n.*25+568_*25+570del
NM_001204307.1:c.*25+568_*25+570del	NP_001191236.1:n.*25+568_*25+570del
XM_006714177.2:c.*39+568_*39+570del	XP_006714240.1:n.*39+568_*39+570del
XM_006714177.3:c.*39+568_*39+570del	XP_006714240.1:n.*39+568_*39+570del
NM_000583.4:c.*25+568_*25+570del MANE Select	NP_000574.2:n.*25+568_*25+570del