Canonical Allele Identifier: CA1266819867
Gene: GGCX HGNC NCBI

Linked Data

dbSNP Id: rs1691635627

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85545841_85545842insTT , CM000664.2:g.85545841_85545842insTT GRCh38
NC_000002.11:g.85772964_85772965insTT , CM000664.1:g.85772964_85772965insTT GRCh37
NC_000002.10:g.85626475_85626476insTT NCBI36
NG_011811.2:g.20694_20695insAA
NG_029183.1:g.11864_11865insTT

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*4093_*4094insAA MANE Select ENSP00000233838.3:n.*4093_*4094insAA
ENST00000233838.8:c.*4093_*4094insAA ENSP00000233838.3:n.*4093_*4094insAA
NM_000821.5:c.*4093_*4094insAA NP_000812.2:n.*4093_*4094insAA
NM_000821.6:c.*4093_*4094insAA NP_000812.2:n.*4093_*4094insAA
NM_001142269.2:c.*4093_*4094insAA NP_001135741.1:n.*4093_*4094insAA
NM_001142269.3:c.*4093_*4094insAA NP_001135741.1:n.*4093_*4094insAA
NM_000821.7:c.*4093_*4094insAA MANE Select NP_000812.2:n.*4093_*4094insAA
NM_001142269.4:c.*4093_*4094insAA NP_001135741.1:n.*4093_*4094insAA