Canonical Allele Identifier: CA798103640

Gene: GC

Linked Data

• dbSNP Id: rs1270039028
• gnomAD v3: 4-71746009-TCG-T
• gnomAD v4: 4-71746009-TCG-T
• MyVariant Identifiers: chr4:g.72611727_72611728del (hg19) ; chr4:g.71746010_71746011del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71746010_71746011del , CM000666.2:g.71746010_71746011del	GRCh38
NC_000004.11:g.72611727_72611728del , CM000666.1:g.72611727_72611728del	GRCh37
NC_000004.10:g.72830591_72830592del	NCBI36
NG_012837.2:g.64510_64511del
NG_012837.3:g.64510_64511del

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.*25+140_*25+141del MANE Select	ENSP00000273951.8:n.*25+140_*25+141del
ENST00000273951.12:c.*25+140_*25+141del	ENSP00000273951.8:n.*25+140_*25+141del
ENST00000503364.5:n.123+140_123+141del
ENST00000503472.5:n.1334+140_1334+141del
ENST00000504199.5:c.*25+140_*25+141del	ENSP00000421725.1:n.*25+140_*25+141del
ENST00000509740.5:c.*273+140_*273+141del	ENSP00000422664.1:n.*273+140_*273+141del
ENST00000513476.5:c.1396-4141_1396-4140del	ENSP00000426683.1:n.1396-4141_1396-4140de...
NM_000583.3:c.*25+140_*25+141del	NP_000574.2:n.*25+140_*25+141del
NM_001204306.1:c.*25+140_*25+141del	NP_001191235.1:n.*25+140_*25+141del
NM_001204307.1:c.*25+140_*25+141del	NP_001191236.1:n.*25+140_*25+141del
XM_006714177.2:c.*39+140_*39+141del	XP_006714240.1:n.*39+140_*39+141del
XM_006714177.3:c.*39+140_*39+141del	XP_006714240.1:n.*39+140_*39+141del
NM_000583.4:c.*25+140_*25+141del MANE Select	NP_000574.2:n.*25+140_*25+141del