Canonical Allele Identifier: CA1467350132
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71743506_71743508delinsACT , CM000666.2:g.71743506_71743508delinsACT GRCh38
NC_000004.11:g.72609223_72609225delinsACT , CM000666.1:g.72609223_72609225delinsACT GRCh37
NC_000004.10:g.72828087_72828089delinsACT NCBI36
NG_012837.2:g.67013_67015delinsAGT
NG_012837.3:g.67013_67015delinsAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.*26-1638_*26-1636delinsAGT MANE Select ENSP00000273951.8:n.*26-1638_*26-1636deli...
ENST00000273951.12:c.*26-1638_*26-1636delinsAGT ENSP00000273951.8:n.*26-1638_*26-1636deli...
ENST00000503364.5:n.124-1638_124-1636delinsAGT
ENST00000503472.5:n.1335-1638_1335-1636delinsAGT
ENST00000504199.5:c.*26-1638_*26-1636delinsAGT ENSP00000421725.1:n.*26-1638_*26-1636deli...
ENST00000509740.5:c.*274-1638_*274-1636delinsAGT ENSP00000422664.1:n.*274-1638_*274-1636de...
ENST00000513476.5:c.1396-1638_1396-1636delinsAGT ENSP00000426683.1:n.1396-1638_1396-1636de...
NM_000583.3:c.*26-1638_*26-1636delinsAGT NP_000574.2:n.*26-1638_*26-1636delinsAGT
NM_001204306.1:c.*26-1638_*26-1636delinsAGT NP_001191235.1:n.*26-1638_*26-1636delinsA...
NM_001204307.1:c.*26-1638_*26-1636delinsAGT NP_001191236.1:n.*26-1638_*26-1636delinsA...
XM_006714177.2:c.*40-1638_*40-1636delinsAGT XP_006714240.1:n.*40-1638_*40-1636delinsA...
XM_006714177.3:c.*40-1638_*40-1636delinsAGT XP_006714240.1:n.*40-1638_*40-1636delinsA...
NM_000583.4:c.*26-1638_*26-1636delinsAGT MANE Select NP_000574.2:n.*26-1638_*26-1636delinsAGT