Canonical Allele Identifier: CA2762138147

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71742258_71742259del , CM000666.2:g.71742258_71742259del	GRCh38
NC_000004.11:g.72607975_72607976del , CM000666.1:g.72607975_72607976del	GRCh37
NC_000004.10:g.72826839_72826840del	NCBI36
NG_012837.2:g.68263_68264del
NG_012837.3:g.68263_68264del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-388_*26-387del MANE Select	ENSP00000273951.8:n.*26-388_*26-387del
ENST00000273951.12:c.*26-388_*26-387del	ENSP00000273951.8:n.*26-388_*26-387del
ENST00000503364.5:n.124-388_124-387del
ENST00000503472.5:n.1335-388_1335-387del
ENST00000504199.5:c.*26-388_*26-387del	ENSP00000421725.1:n.*26-388_*26-387del
ENST00000509740.5:c.*274-388_*274-387del	ENSP00000422664.1:n.*274-388_*274-387del
ENST00000513476.5:c.1396-388_1396-387del	ENSP00000426683.1:n.1396-388_1396-387del
NM_000583.3:c.*26-388_*26-387del	NP_000574.2:n.*26-388_*26-387del
NM_001204306.1:c.*26-388_*26-387del	NP_001191235.1:n.*26-388_*26-387del
NM_001204307.1:c.*26-388_*26-387del	NP_001191236.1:n.*26-388_*26-387del
XM_006714177.2:c.*40-388_*40-387del	XP_006714240.1:n.*40-388_*40-387del
XM_006714177.3:c.*40-388_*40-387del	XP_006714240.1:n.*40-388_*40-387del
NM_000583.4:c.*26-388_*26-387del MANE Select	NP_000574.2:n.*26-388_*26-387del