Canonical Allele Identifier: CA1266825448

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553115_85553116delinsCT , CM000664.2:g.85553115_85553116delinsCT	GRCh38
NC_000002.11:g.85780238_85780239delinsCT , CM000664.1:g.85780238_85780239delinsCT	GRCh37
NC_000002.10:g.85633749_85633750delinsCT	NCBI36
NG_011811.2:g.13419_13420delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5200-46_5200-45delinsAG
ENST00000482662.2:n.3607-46_3607-45delinsAG
ENST00000685865.1:n.1559-46_1559-45delinsAG
ENST00000687250.1:n.1259-46_1259-45delinsAG
ENST00000687995.1:n.1508-46_1508-45delinsAG
ENST00000688205.1:c.*749-46_*749-45delinsAG	ENSP00000509673.1:n.*749-46_*749-45delinsAG
ENST00000688788.1:n.1395-46_1395-45delinsAG
ENST00000689276.1:c.1087-46_1087-45delinsAG	ENSP00000510012.1:n.1087-46_1087-45delinsAG
ENST00000689576.1:c.1156-46_1156-45delinsAG	ENSP00000508712.1:n.1156-46_1156-45delinsAG
ENST00000690108.1:c.*812-46_*812-45delinsAG	ENSP00000510617.1:n.*812-46_*812-45delinsAG
ENST00000690468.1:c.877-46_877-45delinsAG	ENSP00000509078.1:n.877-46_877-45delinsAG
ENST00000690595.1:c.481-46_481-45delinsAG	ENSP00000508979.1:n.481-46_481-45delinsAG
ENST00000691348.1:c.985-46_985-45delinsAG	ENSP00000509369.1:n.985-46_985-45delinsAG
ENST00000691410.1:c.*733-46_*733-45delinsAG	ENSP00000508479.1:n.*733-46_*733-45delinsAG
ENST00000693287.1:c.472-46_472-45delinsAG	ENSP00000510264.1:n.472-46_472-45delinsAG
ENST00000693681.1:c.469-46_469-45delinsAG	ENSP00000510789.1:n.469-46_469-45delinsAG
ENST00000233838.9:c.1156-46_1156-45delinsAG MANE Select	ENSP00000233838.3:n.1156-46_1156-45delinsAG
ENST00000233838.8:c.1156-46_1156-45delinsAG	ENSP00000233838.3:n.1156-46_1156-45delinsAG
ENST00000430215.7:c.985-46_985-45delinsAG	ENSP00000408045.3:n.985-46_985-45delinsAG
ENST00000465637.5:n.179-5112_179-5111delinsAG
ENST00000473665.1:n.649-46_649-45delinsAG
ENST00000482662.1:n.573-46_573-45delinsAG
NM_000821.5:c.1156-46_1156-45delinsAG	NP_000812.2:n.1156-46_1156-45delinsAG
NM_000821.6:c.1156-46_1156-45delinsAG	NP_000812.2:n.1156-46_1156-45delinsAG
NM_001142269.2:c.985-46_985-45delinsAG	NP_001135741.1:n.985-46_985-45delinsAG
NM_001142269.3:c.985-46_985-45delinsAG	NP_001135741.1:n.985-46_985-45delinsAG
XM_005264259.3:c.1156-46_1156-45delinsAG	XP_005264316.1:n.1156-46_1156-45delinsAG
XM_011532764.1:c.334-46_334-45delinsAG	XP_011531066.1:n.334-46_334-45delinsAG
XM_011532765.1:c.334-46_334-45delinsAG	XP_011531067.1:n.334-46_334-45delinsAG
XR_939677.1:n.1221-46_1221-45delinsAG
XM_005264259.5:c.1156-46_1156-45delinsAG	XP_005264316.1:n.1156-46_1156-45delinsAG
XM_011532764.3:c.334-46_334-45delinsAG	XP_011531066.1:n.334-46_334-45delinsAG
XM_011532765.3:c.334-46_334-45delinsAG	XP_011531067.1:n.334-46_334-45delinsAG
XM_017003803.2:c.985-46_985-45delinsAG	XP_016859292.1:n.985-46_985-45delinsAG
XR_001738703.2:n.1221-46_1221-45delinsAG
NM_000821.7:c.1156-46_1156-45delinsAG MANE Select	NP_000812.2:n.1156-46_1156-45delinsAG
NM_001142269.4:c.985-46_985-45delinsAG	NP_001135741.1:n.985-46_985-45delinsAG