Canonical Allele Identifier: CA2659852540

Gene: GGCX

Linked Data

• gnomAD v4: 2-85546531-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546531_85546532insCG , CM000664.2:g.85546531_85546532insCG	GRCh38
NC_000002.11:g.85773654_85773655insCG , CM000664.1:g.85773654_85773655insCG	GRCh37
NC_000002.10:g.85627165_85627166insCG	NCBI36
NG_011811.2:g.20003_20004insCG
NG_029183.1:g.12554_12555insCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*3402_*3403insCG MANE Select	ENSP00000233838.3:n.*3402_*3403insCG
ENST00000233838.8:c.*3402_*3403insCG	ENSP00000233838.3:n.*3402_*3403insCG
NM_000821.5:c.*3402_*3403insCG	NP_000812.2:n.*3402_*3403insCG
NM_000821.6:c.*3402_*3403insCG	NP_000812.2:n.*3402_*3403insCG
NM_001142269.2:c.*3402_*3403insCG	NP_001135741.1:n.*3402_*3403insCG
NM_001142269.3:c.*3402_*3403insCG	NP_001135741.1:n.*3402_*3403insCG
NM_000821.7:c.*3402_*3403insCG MANE Select	NP_000812.2:n.*3402_*3403insCG
NM_001142269.4:c.*3402_*3403insCG	NP_001135741.1:n.*3402_*3403insCG