Canonical Allele Identifier: CA894044484

Gene: GGCX

Linked Data

• dbSNP Id: rs1157892451
• gnomAD v3: 2-85559172-ACTT-A
• gnomAD v4: 2-85559172-ACTT-A
• MyVariant Identifiers: chr2:g.85786296_85786298del (hg19) ; chr2:g.85559173_85559175del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85559176_85559178del , CM000664.2:g.85559176_85559178del	GRCh38
NC_000002.11:g.85786299_85786301del , CM000664.1:g.85786299_85786301del	GRCh37
NC_000002.10:g.85639810_85639812del	NCBI36
NG_011811.2:g.7360_7362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000482662.2:n.282-100_282-98del
ENST00000496962.2:c.215-100_215-98del	ENSP00000508856.1:n.215-100_215-98del
ENST00000685865.1:n.307-100_307-98del
ENST00000687250.1:n.318-100_318-98del
ENST00000687995.1:n.256-100_256-98del
ENST00000688205.1:c.215-100_215-98del	ENSP00000509673.1:n.215-100_215-98del
ENST00000688788.1:n.307-100_307-98del
ENST00000689276.1:c.215-100_215-98del	ENSP00000510012.1:n.215-100_215-98del
ENST00000689576.1:c.215-100_215-98del	ENSP00000508712.1:n.215-100_215-98del
ENST00000690108.1:c.215-100_215-98del	ENSP00000510617.1:n.215-100_215-98del
ENST00000690468.1:c.44-100_44-98del	ENSP00000509078.1:n.44-100_44-98del
ENST00000690595.1:c.214+1640_214+1642del	ENSP00000508979.1:n.214+1640_214+1642del
ENST00000691348.1:c.44-100_44-98del	ENSP00000509369.1:n.44-100_44-98del
ENST00000691410.1:c.215-100_215-98del	ENSP00000508479.1:n.215-100_215-98del
ENST00000693287.1:c.-67+2211_-67+2213del	ENSP00000510264.1:n.-67+2211_-67+2213del
ENST00000693681.1:c.44-100_44-98del	ENSP00000510789.1:n.44-100_44-98del
ENST00000233838.9:c.215-100_215-98del MANE Select	ENSP00000233838.3:n.215-100_215-98del
ENST00000233838.8:c.215-100_215-98del	ENSP00000233838.3:n.215-100_215-98del
ENST00000421496.5:c.44-100_44-98del	ENSP00000400384.1:n.44-100_44-98del
ENST00000423570.5:c.215-100_215-98del	ENSP00000389426.1:n.215-100_215-98del
ENST00000428479.3:c.44-100_44-98del	ENSP00000390748.3:n.44-100_44-98del
ENST00000430215.7:c.44-100_44-98del	ENSP00000408045.3:n.44-100_44-98del
ENST00000465637.5:n.109-100_109-98del
ENST00000481541.1:n.109-100_109-98del
ENST00000496962.1:n.334-100_334-98del
NM_000821.5:c.215-100_215-98del	NP_000812.2:n.215-100_215-98del
NM_000821.6:c.215-100_215-98del	NP_000812.2:n.215-100_215-98del
NM_001142269.2:c.44-100_44-98del	NP_001135741.1:n.44-100_44-98del
NM_001142269.3:c.44-100_44-98del	NP_001135741.1:n.44-100_44-98del
NM_001311312.1:c.215-100_215-98del	NP_001298241.1:n.215-100_215-98del
XM_005264259.3:c.215-100_215-98del	XP_005264316.1:n.215-100_215-98del
XM_011532764.1:c.-444-100_-444-98del	XP_011531066.1:n.-444-100_-444-98del
XM_011532765.1:c.-444-100_-444-98del	XP_011531067.1:n.-444-100_-444-98del
XR_939677.1:n.280-100_280-98del
XM_005264259.5:c.215-100_215-98del	XP_005264316.1:n.215-100_215-98del
XM_011532764.3:c.-444-100_-444-98del	XP_011531066.1:n.-444-100_-444-98del
XM_011532765.3:c.-444-100_-444-98del	XP_011531067.1:n.-444-100_-444-98del
XM_017003803.2:c.44-100_44-98del	XP_016859292.1:n.44-100_44-98del
XR_001738703.2:n.280-100_280-98del
NM_000821.7:c.215-100_215-98del MANE Select	NP_000812.2:n.215-100_215-98del
NM_001142269.4:c.44-100_44-98del	NP_001135741.1:n.44-100_44-98del
NM_001311312.2:c.215-100_215-98del	NP_001298241.1:n.215-100_215-98del