Canonical Allele Identifier: CA1467372715

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755668_71755673delinsATATAT , CM000666.2:g.71755668_71755673delinsATATAT	GRCh38
NC_000004.11:g.72621385_72621390delinsATATAT , CM000666.1:g.72621385_72621390delinsATATAT	GRCh37
NC_000004.10:g.72840249_72840254delinsATATAT	NCBI36
NG_012837.2:g.54848_54853delinsATATAT
NG_012837.3:g.54848_54853delinsATATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1035-566_1035-561delinsATATAT MANE Select	ENSP00000273951.8:n.1035-566_1035-561delinsATATAT
ENST00000273951.12:c.1035-566_1035-561delinsATATAT	ENSP00000273951.8:n.1035-566_1035-561delinsATATAT
ENST00000503472.5:n.919-566_919-561delinsATATAT
ENST00000504199.5:c.1092-566_1092-561delinsATATAT	ENSP00000421725.1:n.1092-566_1092-561delinsATATAT
ENST00000509740.5:c.1034+1039_1034+1044delinsATATAT	ENSP00000422664.1:n.1034+1039_1034+1044delinsATATAT
ENST00000513476.5:c.1035-566_1035-561delinsATATAT	ENSP00000426683.1:n.1035-566_1035-561delinsATATAT
NM_000583.3:c.1035-566_1035-561delinsATATAT	NP_000574.2:n.1035-566_1035-561delinsATATAT
NM_001204306.1:c.1035-566_1035-561delinsATATAT	NP_001191235.1:n.1035-566_1035-561delinsATATAT
NM_001204307.1:c.1092-566_1092-561delinsATATAT	NP_001191236.1:n.1092-566_1092-561delinsATATAT
XM_006714177.2:c.1035-566_1035-561delinsATATAT	XP_006714240.1:n.1035-566_1035-561delinsATATAT
XM_006714177.3:c.1035-566_1035-561delinsATATAT	XP_006714240.1:n.1035-566_1035-561delinsATATAT
NM_000583.4:c.1035-566_1035-561delinsATATAT MANE Select	NP_000574.2:n.1035-566_1035-561delinsATATAT