Canonical Allele Identifier: CA1266819893
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691636843

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545863_85545866dup , CM000664.2:g.85545863_85545866dup GRCh38
NC_000002.11:g.85772986_85772989dup , CM000664.1:g.85772986_85772989dup GRCh37
NC_000002.10:g.85626497_85626500dup NCBI36
NG_011811.2:g.20669_20672dup
NG_029183.1:g.11886_11889dup

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4068_*4071dup MANE Select ENSP00000233838.3:n.*4068_*4071dup
ENST00000233838.8:c.*4068_*4071dup ENSP00000233838.3:n.*4068_*4071dup
NM_000821.5:c.*4068_*4071dup NP_000812.2:n.*4068_*4071dup
NM_000821.6:c.*4068_*4071dup NP_000812.2:n.*4068_*4071dup
NM_001142269.2:c.*4068_*4071dup NP_001135741.1:n.*4068_*4071dup
NM_001142269.3:c.*4068_*4071dup NP_001135741.1:n.*4068_*4071dup
NM_000821.7:c.*4068_*4071dup MANE Select NP_000812.2:n.*4068_*4071dup
NM_001142269.4:c.*4068_*4071dup NP_001135741.1:n.*4068_*4071dup