Canonical Allele Identifier: CA2699812037

Gene: GGCX

Linked Data

• dbSNP Id: rs2103987282

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85559076_85559077insAA , CM000664.2:g.85559076_85559077insAA	GRCh38
NC_000002.11:g.85786199_85786200insAA , CM000664.1:g.85786199_85786200insAA	GRCh37
NC_000002.10:g.85639710_85639711insAA	NCBI36
NG_011811.2:g.7458_7459insTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000482662.2:n.282-2_282-1insTT
ENST00000496962.2:c.215-2_215-1insTT	ENSP00000508856.1:n.215-2_215-1insTT
ENST00000685865.1:n.307-2_307-1insTT
ENST00000687250.1:n.318-2_318-1insTT
ENST00000687995.1:n.256-2_256-1insTT
ENST00000688205.1:c.215-2_215-1insTT	ENSP00000509673.1:n.215-2_215-1insTT
ENST00000688788.1:n.307-2_307-1insTT
ENST00000689276.1:c.215-2_215-1insTT	ENSP00000510012.1:n.215-2_215-1insTT
ENST00000689576.1:c.215-2_215-1insTT	ENSP00000508712.1:n.215-2_215-1insTT
ENST00000690108.1:c.215-2_215-1insTT	ENSP00000510617.1:n.215-2_215-1insTT
ENST00000690468.1:c.44-2_44-1insTT	ENSP00000509078.1:n.44-2_44-1insTT
ENST00000690595.1:c.214+1738_214+1739insTT	ENSP00000508979.1:n.214+1738_214+1739insT...
ENST00000691348.1:c.44-2_44-1insTT	ENSP00000509369.1:n.44-2_44-1insTT
ENST00000691410.1:c.215-2_215-1insTT	ENSP00000508479.1:n.215-2_215-1insTT
ENST00000693287.1:c.-67+2309_-67+2310insTT	ENSP00000510264.1:n.-67+2309_-67+2310insT...
ENST00000693681.1:c.44-2_44-1insTT	ENSP00000510789.1:n.44-2_44-1insTT
ENST00000233838.9:c.215-2_215-1insTT MANE Select	ENSP00000233838.3:n.215-2_215-1insTT
ENST00000233838.8:c.215-2_215-1insTT	ENSP00000233838.3:n.215-2_215-1insTT
ENST00000421496.5:c.44-2_44-1insTT	ENSP00000400384.1:n.44-2_44-1insTT
ENST00000423570.5:c.215-2_215-1insTT	ENSP00000389426.1:n.215-2_215-1insTT
ENST00000428479.3:c.44-2_44-1insTT	ENSP00000390748.3:n.44-2_44-1insTT
ENST00000430215.7:c.44-2_44-1insTT	ENSP00000408045.3:n.44-2_44-1insTT
ENST00000465637.5:n.109-2_109-1insTT
ENST00000481541.1:n.109-2_109-1insTT
ENST00000496962.1:n.334-2_334-1insTT
NM_000821.5:c.215-2_215-1insTT	NP_000812.2:n.215-2_215-1insTT
NM_000821.6:c.215-2_215-1insTT	NP_000812.2:n.215-2_215-1insTT
NM_001142269.2:c.44-2_44-1insTT	NP_001135741.1:n.44-2_44-1insTT
NM_001142269.3:c.44-2_44-1insTT	NP_001135741.1:n.44-2_44-1insTT
NM_001311312.1:c.215-2_215-1insTT	NP_001298241.1:n.215-2_215-1insTT
XM_005264259.3:c.215-2_215-1insTT	XP_005264316.1:n.215-2_215-1insTT
XM_011532764.1:c.-444-2_-444-1insTT	XP_011531066.1:n.-444-2_-444-1insTT
XM_011532765.1:c.-444-2_-444-1insTT	XP_011531067.1:n.-444-2_-444-1insTT
XR_939677.1:n.280-2_280-1insTT
XM_005264259.5:c.215-2_215-1insTT	XP_005264316.1:n.215-2_215-1insTT
XM_011532764.3:c.-444-2_-444-1insTT	XP_011531066.1:n.-444-2_-444-1insTT
XM_011532765.3:c.-444-2_-444-1insTT	XP_011531067.1:n.-444-2_-444-1insTT
XM_017003803.2:c.44-2_44-1insTT	XP_016859292.1:n.44-2_44-1insTT
XR_001738703.2:n.280-2_280-1insTT
NM_000821.7:c.215-2_215-1insTT MANE Select	NP_000812.2:n.215-2_215-1insTT
NM_001142269.4:c.44-2_44-1insTT	NP_001135741.1:n.44-2_44-1insTT
NM_001311312.2:c.215-2_215-1insTT	NP_001298241.1:n.215-2_215-1insTT