Canonical Allele Identifier: CA1467372706

Gene: GC

Linked Data

• dbSNP Id: rs1741744397

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755652del , CM000666.2:g.71755652del	GRCh38
NC_000004.11:g.72621369del , CM000666.1:g.72621369del	GRCh37
NC_000004.10:g.72840233del	NCBI36
NG_012837.2:g.54869del
NG_012837.3:g.54869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1035-545del MANE Select	ENSP00000273951.8:n.1035-545del
ENST00000273951.12:c.1035-545del	ENSP00000273951.8:n.1035-545del
ENST00000503472.5:n.919-545del
ENST00000504199.5:c.1092-545del	ENSP00000421725.1:n.1092-545del
ENST00000509740.5:c.1034+1060del	ENSP00000422664.1:n.1034+1060del
ENST00000513476.5:c.1035-545del	ENSP00000426683.1:n.1035-545del
NM_000583.3:c.1035-545del	NP_000574.2:n.1035-545del
NM_001204306.1:c.1035-545del	NP_001191235.1:n.1035-545del
NM_001204307.1:c.1092-545del	NP_001191236.1:n.1092-545del
XM_006714177.2:c.1035-545del	XP_006714240.1:n.1035-545del
XM_006714177.3:c.1035-545del	XP_006714240.1:n.1035-545del
NM_000583.4:c.1035-545del MANE Select	NP_000574.2:n.1035-545del