Canonical Allele Identifier: CA347485027
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551952T>A , CM000664.2:g.85551952T>A GRCh38
NC_000002.11:g.85779075T>A , CM000664.1:g.85779075T>A GRCh37
NC_000002.10:g.85632586T>A NCBI36
NG_011811.2:g.14583A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000473665.2:n.5947A>T
ENST00000482662.2:n.4354A>T
ENST00000685865.1:n.2306A>T
ENST00000687250.1:n.2006A>T
ENST00000687995.1:n.1821A>T
ENST00000688205.1:c.*1062A>T ENSP00000509673.1:n.*1062A>T
ENST00000688788.1:n.1708A>T
ENST00000689276.1:c.1400A>T ENSP00000510012.1:p.Gln467Leu
ENST00000689576.1:c.*88A>T ENSP00000508712.1:n.*88A>T
ENST00000690108.1:c.*1125A>T ENSP00000510617.1:n.*1125A>T
ENST00000690468.1:c.*21A>T ENSP00000509078.1:n.*21A>T
ENST00000690595.1:c.794A>T ENSP00000508979.1:p.Gln265Leu
ENST00000691348.1:c.*21A>T ENSP00000509369.1:n.*21A>T
ENST00000691410.1:c.*1046A>T ENSP00000508479.1:n.*1046A>T
ENST00000693287.1:c.785A>T ENSP00000510264.1:p.Gln262Leu
ENST00000693681.1:c.782A>T ENSP00000510789.1:p.Gln261Leu
ENST00000233838.9:c.1469A>T MANE Select ENSP00000233838.3:p.Gln490Leu
ENST00000233838.8:c.1469A>T ENSP00000233838.3:p.Gln490Leu
ENST00000430215.7:c.1298A>T ENSP00000408045.3:p.Gln433Leu
ENST00000465637.5:n.179-3948A>T
NM_000821.5:c.1469A>T NP_000812.2:p.Gln490Leu
NM_000821.6:c.1469A>T NP_000812.2:p.Gln490Leu
NM_001142269.2:c.1298A>T NP_001135741.1:p.Gln433Leu
NM_001142269.3:c.1298A>T NP_001135741.1:p.Gln433Leu
XM_005264259.3:c.1469A>T XP_005264316.1:p.Gln490Leu
XM_011532764.1:c.647A>T XP_011531066.1:p.Gln216Leu
XM_011532765.1:c.647A>T XP_011531067.1:p.Gln216Leu
XR_939677.1:n.1382A>T
XM_005264259.5:c.1469A>T XP_005264316.1:p.Gln490Leu
XM_011532764.3:c.647A>T XP_011531066.1:p.Gln216Leu
XM_011532765.3:c.647A>T XP_011531067.1:p.Gln216Leu
XM_017003803.2:c.1298A>T XP_016859292.1:p.Gln433Leu
XR_001738703.2:n.1382A>T
NM_000821.7:c.1469A>T MANE Select NP_000812.2:p.Gln490Leu
NM_001142269.4:c.1298A>T NP_001135741.1:p.Gln433Leu