Canonical Allele Identifier: CA427440119
Gene: GGCX HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.85779068A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551945A>C , CM000664.2:g.85551945A>C GRCh38
NC_000002.11:g.85779068A>C , CM000664.1:g.85779068A>C GRCh37
NC_000002.10:g.85632579A>C NCBI36
NG_011811.2:g.14590T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5954T>G
ENST00000482662.2:n.4361T>G
ENST00000685865.1:n.2313T>G
ENST00000687250.1:n.2013T>G
ENST00000687995.1:n.1828T>G
ENST00000688205.1:c.*1069T>G ENSP00000509673.1:n.*1069T>G
ENST00000688788.1:n.1715T>G
ENST00000689276.1:c.1407T>G ENSP00000510012.1:p.Ala469=
ENST00000689576.1:c.*95T>G ENSP00000508712.1:n.*95T>G
ENST00000690108.1:c.*1132T>G ENSP00000510617.1:n.*1132T>G
ENST00000690468.1:c.*28T>G ENSP00000509078.1:n.*28T>G
ENST00000690595.1:c.801T>G ENSP00000508979.1:p.Ala267=
ENST00000691348.1:c.*28T>G ENSP00000509369.1:n.*28T>G
ENST00000691410.1:c.*1053T>G ENSP00000508479.1:n.*1053T>G
ENST00000693287.1:c.792T>G ENSP00000510264.1:p.Ala264=
ENST00000693681.1:c.789T>G ENSP00000510789.1:p.Ala263=
ENST00000233838.9:c.1476T>G MANE Select ENSP00000233838.3:p.Ala492=
ENST00000233838.8:c.1476T>G ENSP00000233838.3:p.Ala492=
ENST00000430215.7:c.1305T>G ENSP00000408045.3:p.Ala435=
ENST00000465637.5:n.179-3941T>G
NM_000821.5:c.1476T>G NP_000812.2:p.Ala492=
NM_000821.6:c.1476T>G NP_000812.2:p.Ala492=
NM_001142269.2:c.1305T>G NP_001135741.1:p.Ala435=
NM_001142269.3:c.1305T>G NP_001135741.1:p.Ala435=
XM_005264259.3:c.1476T>G XP_005264316.1:p.Ala492=
XM_011532764.1:c.654T>G XP_011531066.1:p.Ala218=
XM_011532765.1:c.654T>G XP_011531067.1:p.Ala218=
XR_939677.1:n.1389T>G
XM_005264259.5:c.1476T>G XP_005264316.1:p.Ala492=
XM_011532764.3:c.654T>G XP_011531066.1:p.Ala218=
XM_011532765.3:c.654T>G XP_011531067.1:p.Ala218=
XM_017003803.2:c.1305T>G XP_016859292.1:p.Ala435=
XR_001738703.2:n.1389T>G
NM_000821.7:c.1476T>G MANE Select NP_000812.2:p.Ala492=
NM_001142269.4:c.1305T>G NP_001135741.1:p.Ala435=