Canonical Allele Identifier: CA2558862249

Gene: GGCX

Linked Data

• gnomAD v4: 2-85546361-T-TGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546362_85546363insAG , CM000664.2:g.85546362_85546363insAG	GRCh38
NC_000002.11:g.85773485_85773486insAG , CM000664.1:g.85773485_85773486insAG	GRCh37
NC_000002.10:g.85626996_85626997insAG	NCBI36
NG_011811.2:g.20173_20174insTC
NG_029183.1:g.12385_12386insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3572_*3573insTC MANE Select	ENSP00000233838.3:n.*3572_*3573insTC
ENST00000233838.8:c.*3572_*3573insTC	ENSP00000233838.3:n.*3572_*3573insTC
NM_000821.5:c.*3572_*3573insTC	NP_000812.2:n.*3572_*3573insTC
NM_000821.6:c.*3572_*3573insTC	NP_000812.2:n.*3572_*3573insTC
NM_001142269.2:c.*3572_*3573insTC	NP_001135741.1:n.*3572_*3573insTC
NM_001142269.3:c.*3572_*3573insTC	NP_001135741.1:n.*3572_*3573insTC
NM_000821.7:c.*3572_*3573insTC MANE Select	NP_000812.2:n.*3572_*3573insTC
NM_001142269.4:c.*3572_*3573insTC	NP_001135741.1:n.*3572_*3573insTC