Canonical Allele Identifier: CA1266821075

Gene: GGCX

Linked Data

• dbSNP Id: rs1691678043
• gnomAD v3: 2-85546602-CAG-C
• gnomAD v4: 2-85546602-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546603_85546604del , CM000664.2:g.85546603_85546604del	GRCh38
NC_000002.11:g.85773726_85773727del , CM000664.1:g.85773726_85773727del	GRCh37
NC_000002.10:g.85627237_85627238del	NCBI36
NG_011811.2:g.19931_19932del
NG_029183.1:g.12626_12627del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3330_*3331del MANE Select	ENSP00000233838.3:n.*3330_*3331del
ENST00000233838.8:c.*3330_*3331del	ENSP00000233838.3:n.*3330_*3331del
NM_000821.5:c.*3330_*3331del	NP_000812.2:n.*3330_*3331del
NM_000821.6:c.*3330_*3331del	NP_000812.2:n.*3330_*3331del
NM_001142269.2:c.*3330_*3331del	NP_001135741.1:n.*3330_*3331del
NM_001142269.3:c.*3330_*3331del	NP_001135741.1:n.*3330_*3331del
NM_000821.7:c.*3330_*3331del MANE Select	NP_000812.2:n.*3330_*3331del
NM_001142269.4:c.*3330_*3331del	NP_001135741.1:n.*3330_*3331del