Canonical Allele Identifier: CA1467349420

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741940_71741941delinsCA , CM000666.2:g.71741940_71741941delinsCA	GRCh38
NC_000004.11:g.72607657_72607658delinsCA , CM000666.1:g.72607657_72607658delinsCA	GRCh37
NC_000004.10:g.72826521_72826522delinsCA	NCBI36
NG_012837.2:g.68580_68581delinsTG
NG_012837.3:g.68580_68581delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-71_*26-70delinsTG MANE Select	ENSP00000273951.8:n.*26-71_*26-70delinsTG
ENST00000273951.12:c.*26-71_*26-70delinsTG	ENSP00000273951.8:n.*26-71_*26-70delinsTG
ENST00000503364.5:n.124-71_124-70delinsTG
ENST00000503472.5:n.1335-71_1335-70delinsTG
ENST00000504199.5:c.*26-71_*26-70delinsTG	ENSP00000421725.1:n.*26-71_*26-70delinsTG
ENST00000509740.5:c.*274-71_*274-70delinsTG	ENSP00000422664.1:n.*274-71_*274-70delinsTG
ENST00000513476.5:c.1396-71_1396-70delinsTG	ENSP00000426683.1:n.1396-71_1396-70delinsTG
NM_000583.3:c.*26-71_*26-70delinsTG	NP_000574.2:n.*26-71_*26-70delinsTG
NM_001204306.1:c.*26-71_*26-70delinsTG	NP_001191235.1:n.*26-71_*26-70delinsTG
NM_001204307.1:c.*26-71_*26-70delinsTG	NP_001191236.1:n.*26-71_*26-70delinsTG
XM_006714177.2:c.*40-71_*40-70delinsTG	XP_006714240.1:n.*40-71_*40-70delinsTG
XM_006714177.3:c.*40-71_*40-70delinsTG	XP_006714240.1:n.*40-71_*40-70delinsTG
NM_000583.4:c.*26-71_*26-70delinsTG MANE Select	NP_000574.2:n.*26-71_*26-70delinsTG