Canonical Allele Identifier: CA2499540143
Gene: GGCX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546869_85546872dup , CM000664.2:g.85546869_85546872dup GRCh38
NC_000002.11:g.85773992_85773995dup , CM000664.1:g.85773992_85773995dup GRCh37
NC_000002.10:g.85627503_85627506dup NCBI36
NG_011811.2:g.19663_19666dup
NG_029183.1:g.12892_12895dup

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3062_*3065dup MANE Select ENSP00000233838.3:n.*3062_*3065dup
ENST00000233838.8:c.*3062_*3065dup ENSP00000233838.3:n.*3062_*3065dup
NM_000821.5:c.*3062_*3065dup NP_000812.2:n.*3062_*3065dup
NM_000821.6:c.*3062_*3065dup NP_000812.2:n.*3062_*3065dup
NM_001142269.2:c.*3062_*3065dup NP_001135741.1:n.*3062_*3065dup
NM_001142269.3:c.*3062_*3065dup NP_001135741.1:n.*3062_*3065dup
NM_000821.7:c.*3062_*3065dup MANE Select NP_000812.2:n.*3062_*3065dup
NM_001142269.4:c.*3062_*3065dup NP_001135741.1:n.*3062_*3065dup
Search 100 bp 5'
Search 100 bp 3'