Canonical Allele Identifier: CA427085363
Gene: GGCX HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.85780140C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85553017C>A , CM000664.2:g.85553017C>A GRCh38
NC_000002.11:g.85780140C>A , CM000664.1:g.85780140C>A GRCh37
NC_000002.10:g.85633651C>A NCBI36
NG_011811.2:g.13518G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5253G>T
ENST00000482662.2:n.3660G>T
ENST00000685865.1:n.1612G>T
ENST00000687250.1:n.1312G>T
ENST00000687995.1:n.1561G>T
ENST00000688205.1:c.*802G>T ENSP00000509673.1:n.*802G>T
ENST00000688788.1:n.1448G>T
ENST00000689276.1:c.1140G>T ENSP00000510012.1:p.Val380=
ENST00000689576.1:c.1209G>T ENSP00000508712.1:p.Val403=
ENST00000690108.1:c.*865G>T ENSP00000510617.1:n.*865G>T
ENST00000690468.1:c.930G>T ENSP00000509078.1:p.Val310=
ENST00000690595.1:c.534G>T ENSP00000508979.1:p.Val178=
ENST00000691348.1:c.1038G>T ENSP00000509369.1:p.Val346=
ENST00000691410.1:c.*786G>T ENSP00000508479.1:n.*786G>T
ENST00000693287.1:c.525G>T ENSP00000510264.1:p.Val175=
ENST00000693681.1:c.522G>T ENSP00000510789.1:p.Val174=
ENST00000233838.9:c.1209G>T MANE Select ENSP00000233838.3:p.Val403=
ENST00000233838.8:c.1209G>T ENSP00000233838.3:p.Val403=
ENST00000430215.7:c.1038G>T ENSP00000408045.3:p.Val346=
ENST00000465637.5:n.179-5013G>T
ENST00000473665.1:n.702G>T
ENST00000482662.1:n.626G>T
NM_000821.5:c.1209G>T NP_000812.2:p.Val403=
NM_000821.6:c.1209G>T NP_000812.2:p.Val403=
NM_001142269.2:c.1038G>T NP_001135741.1:p.Val346=
NM_001142269.3:c.1038G>T NP_001135741.1:p.Val346=
XM_005264259.3:c.1209G>T XP_005264316.1:p.Val403=
XM_011532764.1:c.387G>T XP_011531066.1:p.Val129=
XM_011532765.1:c.387G>T XP_011531067.1:p.Val129=
XR_939677.1:n.1274G>T
XM_005264259.5:c.1209G>T XP_005264316.1:p.Val403=
XM_011532764.3:c.387G>T XP_011531066.1:p.Val129=
XM_011532765.3:c.387G>T XP_011531067.1:p.Val129=
XM_017003803.2:c.1038G>T XP_016859292.1:p.Val346=
XR_001738703.2:n.1274G>T
NM_000821.7:c.1209G>T MANE Select NP_000812.2:p.Val403=
NM_001142269.4:c.1038G>T NP_001135741.1:p.Val346=