Canonical Allele Identifier: CA1266825420

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553058_85553061delinsAGTT , CM000664.2:g.85553058_85553061delinsAGTT	GRCh38
NC_000002.11:g.85780181_85780184delinsAGTT , CM000664.1:g.85780181_85780184delinsAGTT	GRCh37
NC_000002.10:g.85633692_85633695delinsAGTT	NCBI36
NG_011811.2:g.13474_13477delinsAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5209_5212delinsAACT
ENST00000482662.2:n.3616_3619delinsAACT
ENST00000685865.1:n.1568_1571delinsAACT
ENST00000687250.1:n.1268_1271delinsAACT
ENST00000687995.1:n.1517_1520delinsAACT
ENST00000688205.1:c.*758_*761delinsAACT	ENSP00000509673.1:n.*758_*761delinsAACT
ENST00000688788.1:n.1404_1407delinsAACT
ENST00000689276.1:c.1096_1099delinsAACT	ENSP00000510012.1:p.Asn366=
ENST00000689576.1:c.1165_1168delinsAACT	ENSP00000508712.1:p.Asn389=
ENST00000690108.1:c.*821_*824delinsAACT	ENSP00000510617.1:n.*821_*824delinsAACT
ENST00000690468.1:c.886_889delinsAACT	ENSP00000509078.1:p.Asn296=
ENST00000690595.1:c.490_493delinsAACT	ENSP00000508979.1:p.Asn164=
ENST00000691348.1:c.994_997delinsAACT	ENSP00000509369.1:p.Asn332=
ENST00000691410.1:c.*742_*745delinsAACT	ENSP00000508479.1:n.*742_*745delinsAACT
ENST00000693287.1:c.481_484delinsAACT	ENSP00000510264.1:p.Asn161=
ENST00000693681.1:c.478_481delinsAACT	ENSP00000510789.1:p.Asn160=
ENST00000233838.9:c.1165_1168delinsAACT MANE Select	ENSP00000233838.3:p.Asn389=
ENST00000233838.8:c.1165_1168delinsAACT	ENSP00000233838.3:p.Asn389=
ENST00000430215.7:c.994_997delinsAACT	ENSP00000408045.3:p.Asn332=
ENST00000465637.5:n.179-5057_179-5054delinsAACT
ENST00000473665.1:n.658_661delinsAACT
ENST00000482662.1:n.582_585delinsAACT
NM_000821.5:c.1165_1168delinsAACT	NP_000812.2:p.Asn389=
NM_000821.6:c.1165_1168delinsAACT	NP_000812.2:p.Asn389=
NM_001142269.2:c.994_997delinsAACT	NP_001135741.1:p.Asn332=
NM_001142269.3:c.994_997delinsAACT	NP_001135741.1:p.Asn332=
XM_005264259.3:c.1165_1168delinsAACT	XP_005264316.1:p.Asn389=
XM_011532764.1:c.343_346delinsAACT	XP_011531066.1:p.Asn115=
XM_011532765.1:c.343_346delinsAACT	XP_011531067.1:p.Asn115=
XR_939677.1:n.1230_1233delinsAACT
XM_005264259.5:c.1165_1168delinsAACT	XP_005264316.1:p.Asn389=
XM_011532764.3:c.343_346delinsAACT	XP_011531066.1:p.Asn115=
XM_011532765.3:c.343_346delinsAACT	XP_011531067.1:p.Asn115=
XM_017003803.2:c.994_997delinsAACT	XP_016859292.1:p.Asn332=
XR_001738703.2:n.1230_1233delinsAACT
NM_000821.7:c.1165_1168delinsAACT MANE Select	NP_000812.2:p.Asn389=
NM_001142269.4:c.994_997delinsAACT	NP_001135741.1:p.Asn332=