Canonical Allele Identifier: CA1467373951

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71758462_71758496delinsTGAAGAAGTCACAAATGTCTCTTTCTATTCATAAG , CM000666.2:g.71758462_71758496delinsTGAAGAAGTCACAAATGTCTCTTTCTATTCATAAG	GRCh38
NC_000004.11:g.72624179_72624213delinsTGAAGAAGTCACAAATGTCTCTTTCTATTCATAAG , CM000666.1:g.72624179_72624213delinsTGAAGAAGTCACAAATGTCTCTTTCTATTCATAAG	GRCh37
NC_000004.10:g.72843043_72843077delinsTGAAGAAGTCACAAATGTCTCTTTCTATTCATAAG	NCBI36
NG_012837.2:g.52025_52059delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA
NG_012837.3:g.52025_52059delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA MANE Select	ENSP00000273951.8:n.702-325_702-291delinsCTTATGAATAGAAAGAGACA...
ENST00000273951.12:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	ENSP00000273951.8:n.702-325_702-291delinsCTTATGAATAGAAAGAGACA...
ENST00000503472.5:n.586-325_586-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA
ENST00000504199.5:c.759-325_759-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	ENSP00000421725.1:n.759-325_759-291delinsCTTATGAATAGAAAGAGACA...
ENST00000509740.5:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	ENSP00000422664.1:n.702-325_702-291delinsCTTATGAATAGAAAGAGACA...
ENST00000513476.5:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	ENSP00000426683.1:n.702-325_702-291delinsCTTATGAATAGAAAGAGACA...
NM_000583.3:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	NP_000574.2:n.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTG...
NM_001204306.1:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	NP_001191235.1:n.702-325_702-291delinsCTTATGAATAGAAAGAGACATTT...
NM_001204307.1:c.759-325_759-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	NP_001191236.1:n.759-325_759-291delinsCTTATGAATAGAAAGAGACATTT...
XM_006714177.2:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	XP_006714240.1:n.702-325_702-291delinsCTTATGAATAGAAAGAGACATTT...
XM_006714177.3:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA	XP_006714240.1:n.702-325_702-291delinsCTTATGAATAGAAAGAGACATTT...
NM_000583.4:c.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTGACTTCTTCA MANE Select	NP_000574.2:n.702-325_702-291delinsCTTATGAATAGAAAGAGACATTTGTG...