Canonical Allele Identifier: CA2706447729

Gene: GC

Linked Data

• dbSNP Id: rs2149297032

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756916_71756917insCTTTGGCCATGCAATCTTCAGAGGCAGACTCACAGCATTTGGAGAGG , CM000666.2:g.71756916_71756917insCTTTGGCCATGCAATCTTCAGAGGCAGACTCACAGCATTTGGAGAGG	GRCh38
NC_000004.11:g.72622633_72622634insCTTTGGCCATGCAATCTTCAGAGGCAGACTCACAGCATTTGGAGAGG , CM000666.1:g.72622633_72622634insCTTTGGCCATGCAATCTTCAGAGGCAGACTCACAGCATTTGGAGAGG	GRCh37
NC_000004.10:g.72841497_72841498insCTTTGGCCATGCAATCTTCAGAGGCAGACTCACAGCATTTGGAGAGG	NCBI36
NG_012837.2:g.53604_53605insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG
NG_012837.3:g.53604_53605insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG MANE Select	ENSP00000273951.8:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTC...
ENST00000273951.12:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	ENSP00000273951.8:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTC...
ENST00000503472.5:n.716-3_716-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG
ENST00000504199.5:c.889-3_889-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	ENSP00000421725.1:n.889-3_889-2insCCTCTCCAAATGCTGTGAGTCTGCCTC...
ENST00000509740.5:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	ENSP00000422664.1:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTC...
ENST00000513476.5:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	ENSP00000426683.1:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTC...
NM_000583.3:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	NP_000574.2:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGA...
NM_001204306.1:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	NP_001191235.1:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGA...
NM_001204307.1:c.889-3_889-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	NP_001191236.1:n.889-3_889-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGA...
XM_006714177.2:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	XP_006714240.1:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGA...
XM_006714177.3:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG	XP_006714240.1:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGA...
NM_000583.4:c.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGATTGCATGGCCAAAG MANE Select	NP_000574.2:n.832-3_832-2insCCTCTCCAAATGCTGTGAGTCTGCCTCTGAAGA...