Canonical Allele Identifier: CA552288910

Gene: GC

Linked Data

• dbSNP Id: rs1237782389
• gnomAD v2: 4-72607611-TTA-T
• gnomAD v4: 4-71741894-TTA-T
• MyVariant Identifiers: chr4:g.72607612_72607613del (hg19) ; chr4:g.71741895_71741896del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741896_71741897del , CM000666.2:g.71741896_71741897del	GRCh38
NC_000004.11:g.72607613_72607614del , CM000666.1:g.72607613_72607614del	GRCh37
NC_000004.10:g.72826477_72826478del	NCBI36
NG_012837.2:g.68625_68626del
NG_012837.3:g.68625_68626del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-26_*26-25del MANE Select	ENSP00000273951.8:n.*26-26_*26-25del
ENST00000273951.12:c.*26-26_*26-25del	ENSP00000273951.8:n.*26-26_*26-25del
ENST00000503364.5:n.124-26_124-25del
ENST00000503472.5:n.1335-26_1335-25del
ENST00000504199.5:c.*26-26_*26-25del	ENSP00000421725.1:n.*26-26_*26-25del
ENST00000509740.5:c.*274-26_*274-25del	ENSP00000422664.1:n.*274-26_*274-25del
ENST00000513476.5:c.1396-26_1396-25del	ENSP00000426683.1:n.1396-26_1396-25del
NM_000583.3:c.*26-26_*26-25del	NP_000574.2:n.*26-26_*26-25del
NM_001204306.1:c.*26-26_*26-25del	NP_001191235.1:n.*26-26_*26-25del
NM_001204307.1:c.*26-26_*26-25del	NP_001191236.1:n.*26-26_*26-25del
XM_006714177.2:c.*40-26_*40-25del	XP_006714240.1:n.*40-26_*40-25del
XM_006714177.3:c.*40-26_*40-25del	XP_006714240.1:n.*40-26_*40-25del
NM_000583.4:c.*26-26_*26-25del MANE Select	NP_000574.2:n.*26-26_*26-25del