Canonical Allele Identifier: CA1266821519

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546963_85546969delinsTTTAAGG , CM000664.2:g.85546963_85546969delinsTTTAAGG	GRCh38
NC_000002.11:g.85774086_85774092delinsTTTAAGG , CM000664.1:g.85774086_85774092delinsTTTAAGG	GRCh37
NC_000002.10:g.85627597_85627603delinsTTTAAGG	NCBI36
NG_011811.2:g.19566_19572delinsCCTTAAA
NG_029183.1:g.12986_12992delinsTTTAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*2965_*2971delinsCCTTAAA MANE Select	ENSP00000233838.3:n.*2965_*2971delinsCCTTAAA
ENST00000233838.8:c.*2965_*2971delinsCCTTAAA	ENSP00000233838.3:n.*2965_*2971delinsCCTTAAA
NM_000821.5:c.*2965_*2971delinsCCTTAAA	NP_000812.2:n.*2965_*2971delinsCCTTAAA
NM_000821.6:c.*2965_*2971delinsCCTTAAA	NP_000812.2:n.*2965_*2971delinsCCTTAAA
NM_001142269.2:c.*2965_*2971delinsCCTTAAA	NP_001135741.1:n.*2965_*2971delinsCCTTAAA
NM_001142269.3:c.*2965_*2971delinsCCTTAAA	NP_001135741.1:n.*2965_*2971delinsCCTTAAA
NM_000821.7:c.*2965_*2971delinsCCTTAAA MANE Select	NP_000812.2:n.*2965_*2971delinsCCTTAAA
NM_001142269.4:c.*2965_*2971delinsCCTTAAA	NP_001135741.1:n.*2965_*2971delinsCCTTAAA