Canonical Allele Identifier: CA1266821482

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546939_85546942delinsTGAG , CM000664.2:g.85546939_85546942delinsTGAG	GRCh38
NC_000002.11:g.85774062_85774065delinsTGAG , CM000664.1:g.85774062_85774065delinsTGAG	GRCh37
NC_000002.10:g.85627573_85627576delinsTGAG	NCBI36
NG_011811.2:g.19593_19596delinsCTCA
NG_029183.1:g.12962_12965delinsTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*2992_*2995delinsCTCA MANE Select	ENSP00000233838.3:n.*2992_*2995delinsCTCA
ENST00000233838.8:c.*2992_*2995delinsCTCA	ENSP00000233838.3:n.*2992_*2995delinsCTCA
NM_000821.5:c.*2992_*2995delinsCTCA	NP_000812.2:n.*2992_*2995delinsCTCA
NM_000821.6:c.*2992_*2995delinsCTCA	NP_000812.2:n.*2992_*2995delinsCTCA
NM_001142269.2:c.*2992_*2995delinsCTCA	NP_001135741.1:n.*2992_*2995delinsCTCA
NM_001142269.3:c.*2992_*2995delinsCTCA	NP_001135741.1:n.*2992_*2995delinsCTCA
NM_000821.7:c.*2992_*2995delinsCTCA MANE Select	NP_000812.2:n.*2992_*2995delinsCTCA
NM_001142269.4:c.*2992_*2995delinsCTCA	NP_001135741.1:n.*2992_*2995delinsCTCA