Canonical Allele Identifier: CA2659854354
Gene: GGCX HGNC NCBI

Linked Data

gnomAD v4: 2-85553145-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85553145C>A , CM000664.2:g.85553145C>A GRCh38
NC_000002.11:g.85780268C>A , CM000664.1:g.85780268C>A GRCh37
NC_000002.10:g.85633779C>A NCBI36
NG_011811.2:g.13390G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5200-75G>T
ENST00000482662.2:n.3607-75G>T
ENST00000685865.1:n.1559-75G>T
ENST00000687250.1:n.1259-75G>T
ENST00000687995.1:n.1508-75G>T
ENST00000688205.1:c.*749-75G>T ENSP00000509673.1:n.*749-75G>T
ENST00000688788.1:n.1395-75G>T
ENST00000689276.1:c.1087-75G>T ENSP00000510012.1:n.1087-75G>T
ENST00000689576.1:c.1156-75G>T ENSP00000508712.1:n.1156-75G>T
ENST00000690108.1:c.*812-75G>T ENSP00000510617.1:n.*812-75G>T
ENST00000690468.1:c.877-75G>T ENSP00000509078.1:n.877-75G>T
ENST00000690595.1:c.481-75G>T ENSP00000508979.1:n.481-75G>T
ENST00000691348.1:c.985-75G>T ENSP00000509369.1:n.985-75G>T
ENST00000691410.1:c.*733-75G>T ENSP00000508479.1:n.*733-75G>T
ENST00000693287.1:c.472-75G>T ENSP00000510264.1:n.472-75G>T
ENST00000693681.1:c.469-75G>T ENSP00000510789.1:n.469-75G>T
ENST00000233838.9:c.1156-75G>T MANE Select ENSP00000233838.3:n.1156-75G>T
ENST00000233838.8:c.1156-75G>T ENSP00000233838.3:n.1156-75G>T
ENST00000430215.7:c.985-75G>T ENSP00000408045.3:n.985-75G>T
ENST00000465637.5:n.179-5141G>T
ENST00000473665.1:n.649-75G>T
ENST00000482662.1:n.573-75G>T
NM_000821.5:c.1156-75G>T NP_000812.2:n.1156-75G>T
NM_000821.6:c.1156-75G>T NP_000812.2:n.1156-75G>T
NM_001142269.2:c.985-75G>T NP_001135741.1:n.985-75G>T
NM_001142269.3:c.985-75G>T NP_001135741.1:n.985-75G>T
XM_005264259.3:c.1156-75G>T XP_005264316.1:n.1156-75G>T
XM_011532764.1:c.334-75G>T XP_011531066.1:n.334-75G>T
XM_011532765.1:c.334-75G>T XP_011531067.1:n.334-75G>T
XR_939677.1:n.1221-75G>T
XM_005264259.5:c.1156-75G>T XP_005264316.1:n.1156-75G>T
XM_011532764.3:c.334-75G>T XP_011531066.1:n.334-75G>T
XM_011532765.3:c.334-75G>T XP_011531067.1:n.334-75G>T
XM_017003803.2:c.985-75G>T XP_016859292.1:n.985-75G>T
XR_001738703.2:n.1221-75G>T
NM_000821.7:c.1156-75G>T MANE Select NP_000812.2:n.1156-75G>T
NM_001142269.4:c.985-75G>T NP_001135741.1:n.985-75G>T