Canonical Allele Identifier: CA2670940905

Gene: GC

Linked Data

• gnomAD v4: 4-71742007-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71742007_71742008insT , CM000666.2:g.71742007_71742008insT	GRCh38
NC_000004.11:g.72607724_72607725insT , CM000666.1:g.72607724_72607725insT	GRCh37
NC_000004.10:g.72826588_72826589insT	NCBI36
NG_012837.2:g.68513_68514insA
NG_012837.3:g.68513_68514insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*26-138_*26-137insA MANE Select	ENSP00000273951.8:n.*26-138_*26-137insA
ENST00000273951.12:c.*26-138_*26-137insA	ENSP00000273951.8:n.*26-138_*26-137insA
ENST00000503364.5:n.124-138_124-137insA
ENST00000503472.5:n.1335-138_1335-137insA
ENST00000504199.5:c.*26-138_*26-137insA	ENSP00000421725.1:n.*26-138_*26-137insA
ENST00000509740.5:c.*274-138_*274-137insA	ENSP00000422664.1:n.*274-138_*274-137insA
ENST00000513476.5:c.1396-138_1396-137insA	ENSP00000426683.1:n.1396-138_1396-137insA
NM_000583.3:c.*26-138_*26-137insA	NP_000574.2:n.*26-138_*26-137insA
NM_001204306.1:c.*26-138_*26-137insA	NP_001191235.1:n.*26-138_*26-137insA
NM_001204307.1:c.*26-138_*26-137insA	NP_001191236.1:n.*26-138_*26-137insA
XM_006714177.2:c.*40-138_*40-137insA	XP_006714240.1:n.*40-138_*40-137insA
XM_006714177.3:c.*40-138_*40-137insA	XP_006714240.1:n.*40-138_*40-137insA
NM_000583.4:c.*26-138_*26-137insA MANE Select	NP_000574.2:n.*26-138_*26-137insA