Canonical Allele Identifier: CA1266821480
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546939_85546941delinsTGA , CM000664.2:g.85546939_85546941delinsTGA GRCh38
NC_000002.11:g.85774062_85774064delinsTGA , CM000664.1:g.85774062_85774064delinsTGA GRCh37
NC_000002.10:g.85627573_85627575delinsTGA NCBI36
NG_011811.2:g.19594_19596delinsTCA
NG_029183.1:g.12962_12964delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*2993_*2995delinsTCA MANE Select ENSP00000233838.3:n.*2993_*2995delinsTCA
ENST00000233838.8:c.*2993_*2995delinsTCA ENSP00000233838.3:n.*2993_*2995delinsTCA
NM_000821.5:c.*2993_*2995delinsTCA NP_000812.2:n.*2993_*2995delinsTCA
NM_000821.6:c.*2993_*2995delinsTCA NP_000812.2:n.*2993_*2995delinsTCA
NM_001142269.2:c.*2993_*2995delinsTCA NP_001135741.1:n.*2993_*2995delinsTCA
NM_001142269.3:c.*2993_*2995delinsTCA NP_001135741.1:n.*2993_*2995delinsTCA
NM_000821.7:c.*2993_*2995delinsTCA MANE Select NP_000812.2:n.*2993_*2995delinsTCA
NM_001142269.4:c.*2993_*2995delinsTCA NP_001135741.1:n.*2993_*2995delinsTCA