Canonical Allele Identifier: CA1266820646
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546377_85546380delinsCGTG , CM000664.2:g.85546377_85546380delinsCGTG GRCh38
NC_000002.11:g.85773500_85773503delinsCGTG , CM000664.1:g.85773500_85773503delinsCGTG GRCh37
NC_000002.10:g.85627011_85627014delinsCGTG NCBI36
NG_011811.2:g.20155_20158delinsCACG
NG_029183.1:g.12400_12403delinsCGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233838.9:c.*3554_*3557delinsCACG MANE Select ENSP00000233838.3:n.*3554_*3557delinsCACG
ENST00000233838.8:c.*3554_*3557delinsCACG ENSP00000233838.3:n.*3554_*3557delinsCACG
NM_000821.5:c.*3554_*3557delinsCACG NP_000812.2:n.*3554_*3557delinsCACG
NM_000821.6:c.*3554_*3557delinsCACG NP_000812.2:n.*3554_*3557delinsCACG
NM_001142269.2:c.*3554_*3557delinsCACG NP_001135741.1:n.*3554_*3557delinsCACG
NM_001142269.3:c.*3554_*3557delinsCACG NP_001135741.1:n.*3554_*3557delinsCACG
NM_000821.7:c.*3554_*3557delinsCACG MANE Select NP_000812.2:n.*3554_*3557delinsCACG
NM_001142269.4:c.*3554_*3557delinsCACG NP_001135741.1:n.*3554_*3557delinsCACG