Canonical Allele Identifier: CA1467372792

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71755838_71755848delinsACTTATAAAAG , CM000666.2:g.71755838_71755848delinsACTTATAAAAG	GRCh38
NC_000004.11:g.72621555_72621565delinsACTTATAAAAG , CM000666.1:g.72621555_72621565delinsACTTATAAAAG	GRCh37
NC_000004.10:g.72840419_72840429delinsACTTATAAAAG	NCBI36
NG_012837.2:g.54673_54683delinsCTTTTATAAGT
NG_012837.3:g.54673_54683delinsCTTTTATAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.1035-741_1035-731delinsCTTTTATAAGT MANE Select	ENSP00000273951.8:n.1035-741_1035-731delinsCTTTTATAAGT
ENST00000273951.12:c.1035-741_1035-731delinsCTTTTATAAGT	ENSP00000273951.8:n.1035-741_1035-731delinsCTTTTATAAGT
ENST00000503472.5:n.919-741_919-731delinsCTTTTATAAGT
ENST00000504199.5:c.1092-741_1092-731delinsCTTTTATAAGT	ENSP00000421725.1:n.1092-741_1092-731delinsCTTTTATAAGT
ENST00000509740.5:c.1034+864_1034+874delinsCTTTTATAAGT	ENSP00000422664.1:n.1034+864_1034+874delinsCTTTTATAAGT
ENST00000513476.5:c.1035-741_1035-731delinsCTTTTATAAGT	ENSP00000426683.1:n.1035-741_1035-731delinsCTTTTATAAGT
NM_000583.3:c.1035-741_1035-731delinsCTTTTATAAGT	NP_000574.2:n.1035-741_1035-731delinsCTTTTATAAGT
NM_001204306.1:c.1035-741_1035-731delinsCTTTTATAAGT	NP_001191235.1:n.1035-741_1035-731delinsCTTTTATAAGT
NM_001204307.1:c.1092-741_1092-731delinsCTTTTATAAGT	NP_001191236.1:n.1092-741_1092-731delinsCTTTTATAAGT
XM_006714177.2:c.1035-741_1035-731delinsCTTTTATAAGT	XP_006714240.1:n.1035-741_1035-731delinsCTTTTATAAGT
XM_006714177.3:c.1035-741_1035-731delinsCTTTTATAAGT	XP_006714240.1:n.1035-741_1035-731delinsCTTTTATAAGT
NM_000583.4:c.1035-741_1035-731delinsCTTTTATAAGT MANE Select	NP_000574.2:n.1035-741_1035-731delinsCTTTTATAAGT