Canonical Allele Identifier: CA1467349367

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741827_71741850delinsTTAGGTCATCAGAGATCATTCCCC , CM000666.2:g.71741827_71741850delinsTTAGGTCATCAGAGATCATTCCCC	GRCh38
NC_000004.11:g.72607544_72607567delinsTTAGGTCATCAGAGATCATTCCCC , CM000666.1:g.72607544_72607567delinsTTAGGTCATCAGAGATCATTCCCC	GRCh37
NC_000004.10:g.72826408_72826431delinsTTAGGTCATCAGAGATCATTCCCC	NCBI36
NG_012837.2:g.68671_68694delinsGGGGAATGATCTCTGATGACCTAA
NG_012837.3:g.68671_68694delinsGGGGAATGATCTCTGATGACCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*46_*69delinsGGGGAATGATCTCTGATGACCTAA MANE Select	ENSP00000273951.8:n.*46_*69delinsGGGGAATGATCTCTGATGACCTAA
ENST00000273951.12:c.*46_*69delinsGGGGAATGATCTCTGATGACCTAA	ENSP00000273951.8:n.*46_*69delinsGGGGAATGATCTCTGATGACCTAA
ENST00000503364.5:n.144_167delinsGGGGAATGATCTCTGATGACCTAA
ENST00000503472.5:n.1355_1378delinsGGGGAATGATCTCTGATGACCTAA
ENST00000504199.5:c.*46_*69delinsGGGGAATGATCTCTGATGACCTAA	ENSP00000421725.1:n.*46_*69delinsGGGGAATGATCTCTGATGACCTAA
ENST00000509740.5:c.*294_*317delinsGGGGAATGATCTCTGATGACCTAA	ENSP00000422664.1:n.*294_*317delinsGGGGAATGATCTCTGATGACCTAA
ENST00000513476.5:c.1416_*8delinsGGGGAATGATCTCTGATGACCTAA	ENSP00000426683.1:n.[c.1416_*8delinsGGGGAATGATCTCTGATGACCTAA;...
NM_000583.3:c.*46_*69delinsGGGGAATGATCTCTGATGACCTAA	NP_000574.2:n.*46_*69delinsGGGGAATGATCTCTGATGACCTAA
NM_001204306.1:c.*46_*69delinsGGGGAATGATCTCTGATGACCTAA	NP_001191235.1:n.*46_*69delinsGGGGAATGATCTCTGATGACCTAA
NM_001204307.1:c.*46_*69delinsGGGGAATGATCTCTGATGACCTAA	NP_001191236.1:n.*46_*69delinsGGGGAATGATCTCTGATGACCTAA
XM_006714177.2:c.*60_*83delinsGGGGAATGATCTCTGATGACCTAA	XP_006714240.1:n.*60_*83delinsGGGGAATGATCTCTGATGACCTAA
XM_006714177.3:c.*60_*83delinsGGGGAATGATCTCTGATGACCTAA	XP_006714240.1:n.*60_*83delinsGGGGAATGATCTCTGATGACCTAA
NM_000583.4:c.*46_*69delinsGGGGAATGATCTCTGATGACCTAA MANE Select	NP_000574.2:n.*46_*69delinsGGGGAATGATCTCTGATGACCTAA