Canonical Allele Identifier: CA1467372806
Gene: GC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71755870_71755872delinsTAA , CM000666.2:g.71755870_71755872delinsTAA GRCh38
NC_000004.11:g.72621587_72621589delinsTAA , CM000666.1:g.72621587_72621589delinsTAA GRCh37
NC_000004.10:g.72840451_72840453delinsTAA NCBI36
NG_012837.2:g.54649_54651delinsTTA
NG_012837.3:g.54649_54651delinsTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.1035-765_1035-763delinsTTA MANE Select ENSP00000273951.8:n.1035-765_1035-763deli...
ENST00000273951.12:c.1035-765_1035-763delinsTTA ENSP00000273951.8:n.1035-765_1035-763deli...
ENST00000503472.5:n.919-765_919-763delinsTTA
ENST00000504199.5:c.1092-765_1092-763delinsTTA ENSP00000421725.1:n.1092-765_1092-763deli...
ENST00000509740.5:c.1034+840_1034+842delinsTTA ENSP00000422664.1:n.1034+840_1034+842deli...
ENST00000513476.5:c.1035-765_1035-763delinsTTA ENSP00000426683.1:n.1035-765_1035-763deli...
NM_000583.3:c.1035-765_1035-763delinsTTA NP_000574.2:n.1035-765_1035-763delinsTTA
NM_001204306.1:c.1035-765_1035-763delinsTTA NP_001191235.1:n.1035-765_1035-763delinsT...
NM_001204307.1:c.1092-765_1092-763delinsTTA NP_001191236.1:n.1092-765_1092-763delinsT...
XM_006714177.2:c.1035-765_1035-763delinsTTA XP_006714240.1:n.1035-765_1035-763delinsT...
XM_006714177.3:c.1035-765_1035-763delinsTTA XP_006714240.1:n.1035-765_1035-763delinsT...
NM_000583.4:c.1035-765_1035-763delinsTTA MANE Select NP_000574.2:n.1035-765_1035-763delinsTTA