Canonical Allele Identifier: CA1266820726
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85546405_85546409delinsAGAGT , CM000664.2:g.85546405_85546409delinsAGAGT GRCh38
NC_000002.11:g.85773528_85773532delinsAGAGT , CM000664.1:g.85773528_85773532delinsAGAGT GRCh37
NC_000002.10:g.85627039_85627043delinsAGAGT NCBI36
NG_011811.2:g.20126_20130delinsACTCT
NG_029183.1:g.12428_12432delinsAGAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000233838.9:c.*3525_*3529delinsACTCT MANE Select ENSP00000233838.3:n.*3525_*3529delinsACTC...
ENST00000233838.8:c.*3525_*3529delinsACTCT ENSP00000233838.3:n.*3525_*3529delinsACTC...
NM_000821.5:c.*3525_*3529delinsACTCT NP_000812.2:n.*3525_*3529delinsACTCT
NM_000821.6:c.*3525_*3529delinsACTCT NP_000812.2:n.*3525_*3529delinsACTCT
NM_001142269.2:c.*3525_*3529delinsACTCT NP_001135741.1:n.*3525_*3529delinsACTCT
NM_001142269.3:c.*3525_*3529delinsACTCT NP_001135741.1:n.*3525_*3529delinsACTCT
NM_000821.7:c.*3525_*3529delinsACTCT MANE Select NP_000812.2:n.*3525_*3529delinsACTCT
NM_001142269.4:c.*3525_*3529delinsACTCT NP_001135741.1:n.*3525_*3529delinsACTCT