Canonical Allele Identifier: CA2659854327

Gene: GGCX

Linked Data

• gnomAD v4: 2-85553110-TCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553114_85553115del , CM000664.2:g.85553114_85553115del	GRCh38
NC_000002.11:g.85780237_85780238del , CM000664.1:g.85780237_85780238del	GRCh37
NC_000002.10:g.85633748_85633749del	NCBI36
NG_011811.2:g.13423_13424del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5200-42_5200-41del
ENST00000482662.2:n.3607-42_3607-41del
ENST00000685865.1:n.1559-42_1559-41del
ENST00000687250.1:n.1259-42_1259-41del
ENST00000687995.1:n.1508-42_1508-41del
ENST00000688205.1:c.*749-42_*749-41del	ENSP00000509673.1:n.*749-42_*749-41del
ENST00000688788.1:n.1395-42_1395-41del
ENST00000689276.1:c.1087-42_1087-41del	ENSP00000510012.1:n.1087-42_1087-41del
ENST00000689576.1:c.1156-42_1156-41del	ENSP00000508712.1:n.1156-42_1156-41del
ENST00000690108.1:c.*812-42_*812-41del	ENSP00000510617.1:n.*812-42_*812-41del
ENST00000690468.1:c.877-42_877-41del	ENSP00000509078.1:n.877-42_877-41del
ENST00000690595.1:c.481-42_481-41del	ENSP00000508979.1:n.481-42_481-41del
ENST00000691348.1:c.985-42_985-41del	ENSP00000509369.1:n.985-42_985-41del
ENST00000691410.1:c.*733-42_*733-41del	ENSP00000508479.1:n.*733-42_*733-41del
ENST00000693287.1:c.472-42_472-41del	ENSP00000510264.1:n.472-42_472-41del
ENST00000693681.1:c.469-42_469-41del	ENSP00000510789.1:n.469-42_469-41del
ENST00000233838.9:c.1156-42_1156-41del MANE Select	ENSP00000233838.3:n.1156-42_1156-41del
ENST00000233838.8:c.1156-42_1156-41del	ENSP00000233838.3:n.1156-42_1156-41del
ENST00000430215.7:c.985-42_985-41del	ENSP00000408045.3:n.985-42_985-41del
ENST00000465637.5:n.179-5108_179-5107del
ENST00000473665.1:n.649-42_649-41del
ENST00000482662.1:n.573-42_573-41del
NM_000821.5:c.1156-42_1156-41del	NP_000812.2:n.1156-42_1156-41del
NM_000821.6:c.1156-42_1156-41del	NP_000812.2:n.1156-42_1156-41del
NM_001142269.2:c.985-42_985-41del	NP_001135741.1:n.985-42_985-41del
NM_001142269.3:c.985-42_985-41del	NP_001135741.1:n.985-42_985-41del
XM_005264259.3:c.1156-42_1156-41del	XP_005264316.1:n.1156-42_1156-41del
XM_011532764.1:c.334-42_334-41del	XP_011531066.1:n.334-42_334-41del
XM_011532765.1:c.334-42_334-41del	XP_011531067.1:n.334-42_334-41del
XR_939677.1:n.1221-42_1221-41del
XM_005264259.5:c.1156-42_1156-41del	XP_005264316.1:n.1156-42_1156-41del
XM_011532764.3:c.334-42_334-41del	XP_011531066.1:n.334-42_334-41del
XM_011532765.3:c.334-42_334-41del	XP_011531067.1:n.334-42_334-41del
XM_017003803.2:c.985-42_985-41del	XP_016859292.1:n.985-42_985-41del
XR_001738703.2:n.1221-42_1221-41del
NM_000821.7:c.1156-42_1156-41del MANE Select	NP_000812.2:n.1156-42_1156-41del
NM_001142269.4:c.985-42_985-41del	NP_001135741.1:n.985-42_985-41del