Canonical Allele Identifier: CA1266822740
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85547890_85547892delinsGAT , CM000664.2:g.85547890_85547892delinsGAT GRCh38
NC_000002.11:g.85775013_85775015delinsGAT , CM000664.1:g.85775013_85775015delinsGAT GRCh37
NC_000002.10:g.85628524_85628526delinsGAT NCBI36
NG_011811.2:g.18643_18645delinsATC

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*2042_*2044delinsATC MANE Select ENSP00000233838.3:n.*2042_*2044delinsATC
ENST00000233838.8:c.*2042_*2044delinsATC ENSP00000233838.3:n.*2042_*2044delinsATC
ENST00000465637.5:n.291_293delinsATC
NM_000821.5:c.*2042_*2044delinsATC NP_000812.2:n.*2042_*2044delinsATC
NM_000821.6:c.*2042_*2044delinsATC NP_000812.2:n.*2042_*2044delinsATC
NM_001142269.2:c.*2042_*2044delinsATC NP_001135741.1:n.*2042_*2044delinsATC
NM_001142269.3:c.*2042_*2044delinsATC NP_001135741.1:n.*2042_*2044delinsATC
NM_000821.7:c.*2042_*2044delinsATC MANE Select NP_000812.2:n.*2042_*2044delinsATC
NM_001142269.4:c.*2042_*2044delinsATC NP_001135741.1:n.*2042_*2044delinsATC
Search 100 bp 5'
Search 100 bp 3'