Canonical Allele Identifier: CA1266820625

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546368_85546377delinsAGCTGAAATC , CM000664.2:g.85546368_85546377delinsAGCTGAAATC	GRCh38
NC_000002.11:g.85773491_85773500delinsAGCTGAAATC , CM000664.1:g.85773491_85773500delinsAGCTGAAATC	GRCh37
NC_000002.10:g.85627002_85627011delinsAGCTGAAATC	NCBI36
NG_011811.2:g.20158_20167delinsGATTTCAGCT
NG_029183.1:g.12391_12400delinsAGCTGAAATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3557_*3566delinsGATTTCAGCT MANE Select	ENSP00000233838.3:n.*3557_*3566delinsGATTTCAGCT
ENST00000233838.8:c.*3557_*3566delinsGATTTCAGCT	ENSP00000233838.3:n.*3557_*3566delinsGATTTCAGCT
NM_000821.5:c.*3557_*3566delinsGATTTCAGCT	NP_000812.2:n.*3557_*3566delinsGATTTCAGCT
NM_000821.6:c.*3557_*3566delinsGATTTCAGCT	NP_000812.2:n.*3557_*3566delinsGATTTCAGCT
NM_001142269.2:c.*3557_*3566delinsGATTTCAGCT	NP_001135741.1:n.*3557_*3566delinsGATTTCAGCT
NM_001142269.3:c.*3557_*3566delinsGATTTCAGCT	NP_001135741.1:n.*3557_*3566delinsGATTTCAGCT
NM_000821.7:c.*3557_*3566delinsGATTTCAGCT MANE Select	NP_000812.2:n.*3557_*3566delinsGATTTCAGCT
NM_001142269.4:c.*3557_*3566delinsGATTTCAGCT	NP_001135741.1:n.*3557_*3566delinsGATTTCAGCT