Canonical Allele Identifier: CA2762138202

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71743478_71743480del , CM000666.2:g.71743478_71743480del	GRCh38
NC_000004.11:g.72609195_72609197del , CM000666.1:g.72609195_72609197del	GRCh37
NC_000004.10:g.72828059_72828061del	NCBI36
NG_012837.2:g.67043_67045del
NG_012837.3:g.67043_67045del

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.*26-1608_*26-1606del MANE Select	ENSP00000273951.8:n.*26-1608_*26-1606del
ENST00000273951.12:c.*26-1608_*26-1606del	ENSP00000273951.8:n.*26-1608_*26-1606del
ENST00000503364.5:n.124-1608_124-1606del
ENST00000503472.5:n.1335-1608_1335-1606del
ENST00000504199.5:c.*26-1608_*26-1606del	ENSP00000421725.1:n.*26-1608_*26-1606del
ENST00000509740.5:c.*274-1608_*274-1606del	ENSP00000422664.1:n.*274-1608_*274-1606del
ENST00000513476.5:c.1396-1608_1396-1606del	ENSP00000426683.1:n.1396-1608_1396-1606del
NM_000583.3:c.*26-1608_*26-1606del	NP_000574.2:n.*26-1608_*26-1606del
NM_001204306.1:c.*26-1608_*26-1606del	NP_001191235.1:n.*26-1608_*26-1606del
NM_001204307.1:c.*26-1608_*26-1606del	NP_001191236.1:n.*26-1608_*26-1606del
XM_006714177.2:c.*40-1608_*40-1606del	XP_006714240.1:n.*40-1608_*40-1606del
XM_006714177.3:c.*40-1608_*40-1606del	XP_006714240.1:n.*40-1608_*40-1606del
NM_000583.4:c.*26-1608_*26-1606del MANE Select	NP_000574.2:n.*26-1608_*26-1606del