Canonical Allele Identifier: CA1467349866

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71742920_71742921delinsGC , CM000666.2:g.71742920_71742921delinsGC	GRCh38
NC_000004.11:g.72608637_72608638delinsGC , CM000666.1:g.72608637_72608638delinsGC	GRCh37
NC_000004.10:g.72827501_72827502delinsGC	NCBI36
NG_012837.2:g.67600_67601delinsGC
NG_012837.3:g.67600_67601delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-1051_*26-1050delinsGC MANE Select	ENSP00000273951.8:n.*26-1051_*26-1050delinsGC
ENST00000273951.12:c.*26-1051_*26-1050delinsGC	ENSP00000273951.8:n.*26-1051_*26-1050delinsGC
ENST00000503364.5:n.124-1051_124-1050delinsGC
ENST00000503472.5:n.1335-1051_1335-1050delinsGC
ENST00000504199.5:c.*26-1051_*26-1050delinsGC	ENSP00000421725.1:n.*26-1051_*26-1050delinsGC
ENST00000509740.5:c.*274-1051_*274-1050delinsGC	ENSP00000422664.1:n.*274-1051_*274-1050delinsGC
ENST00000513476.5:c.1396-1051_1396-1050delinsGC	ENSP00000426683.1:n.1396-1051_1396-1050delinsGC
NM_000583.3:c.*26-1051_*26-1050delinsGC	NP_000574.2:n.*26-1051_*26-1050delinsGC
NM_001204306.1:c.*26-1051_*26-1050delinsGC	NP_001191235.1:n.*26-1051_*26-1050delinsGC
NM_001204307.1:c.*26-1051_*26-1050delinsGC	NP_001191236.1:n.*26-1051_*26-1050delinsGC
XM_006714177.2:c.*40-1051_*40-1050delinsGC	XP_006714240.1:n.*40-1051_*40-1050delinsGC
XM_006714177.3:c.*40-1051_*40-1050delinsGC	XP_006714240.1:n.*40-1051_*40-1050delinsGC
NM_000583.4:c.*26-1051_*26-1050delinsGC MANE Select	NP_000574.2:n.*26-1051_*26-1050delinsGC