Canonical Allele Identifier: CA99057447

Gene: GC

Linked Data

• dbSNP Id: rs887952932
• gnomAD v3: 4-71742127-TG-T
• gnomAD v4: 4-71742127-TG-T
• MyVariant Identifiers: chr4:g.72607845del (hg19) ; chr4:g.71742128del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71742128del , CM000666.2:g.71742128del	GRCh38
NC_000004.11:g.72607845del , CM000666.1:g.72607845del	GRCh37
NC_000004.10:g.72826709del	NCBI36
NG_012837.2:g.68393del
NG_012837.3:g.68393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-258del MANE Select	ENSP00000273951.8:n.*26-258del
ENST00000273951.12:c.*26-258del	ENSP00000273951.8:n.*26-258del
ENST00000503364.5:n.124-258del
ENST00000503472.5:n.1335-258del
ENST00000504199.5:c.*26-258del	ENSP00000421725.1:n.*26-258del
ENST00000509740.5:c.*274-258del	ENSP00000422664.1:n.*274-258del
ENST00000513476.5:c.1396-258del	ENSP00000426683.1:n.1396-258del
NM_000583.3:c.*26-258del	NP_000574.2:n.*26-258del
NM_001204306.1:c.*26-258del	NP_001191235.1:n.*26-258del
NM_001204307.1:c.*26-258del	NP_001191236.1:n.*26-258del
XM_006714177.2:c.*40-258del	XP_006714240.1:n.*40-258del
XM_006714177.3:c.*40-258del	XP_006714240.1:n.*40-258del
NM_000583.4:c.*26-258del MANE Select	NP_000574.2:n.*26-258del