Canonical Allele Identifier: CA798110329

Gene: GC

Linked Data

• dbSNP Id: rs1209630276
• gnomAD v3: 4-71755810-TTA-T
• gnomAD v4: 4-71755810-TTA-T
• MyVariant Identifiers: chr4:g.72621528_72621529del (hg19) ; chr4:g.71755811_71755812del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755812_71755813del , CM000666.2:g.71755812_71755813del	GRCh38
NC_000004.11:g.72621529_72621530del , CM000666.1:g.72621529_72621530del	GRCh37
NC_000004.10:g.72840393_72840394del	NCBI36
NG_012837.2:g.54709_54710del
NG_012837.3:g.54709_54710del

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.1035-705_1035-704del MANE Select	ENSP00000273951.8:n.1035-705_1035-704del
ENST00000273951.12:c.1035-705_1035-704del	ENSP00000273951.8:n.1035-705_1035-704del
ENST00000503472.5:n.919-705_919-704del
ENST00000504199.5:c.1092-705_1092-704del	ENSP00000421725.1:n.1092-705_1092-704del
ENST00000509740.5:c.1034+900_1034+901del	ENSP00000422664.1:n.1034+900_1034+901del
ENST00000513476.5:c.1035-705_1035-704del	ENSP00000426683.1:n.1035-705_1035-704del
NM_000583.3:c.1035-705_1035-704del	NP_000574.2:n.1035-705_1035-704del
NM_001204306.1:c.1035-705_1035-704del	NP_001191235.1:n.1035-705_1035-704del
NM_001204307.1:c.1092-705_1092-704del	NP_001191236.1:n.1092-705_1092-704del
XM_006714177.2:c.1035-705_1035-704del	XP_006714240.1:n.1035-705_1035-704del
XM_006714177.3:c.1035-705_1035-704del	XP_006714240.1:n.1035-705_1035-704del
NM_000583.4:c.1035-705_1035-704del MANE Select	NP_000574.2:n.1035-705_1035-704del