Canonical Allele Identifier: CA347487326

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780368T>A (hg19) ; chr2:g.85553245T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553245T>A , CM000664.2:g.85553245T>A	GRCh38
NC_000002.11:g.85780368T>A , CM000664.1:g.85780368T>A	GRCh37
NC_000002.10:g.85633879T>A	NCBI36
NG_011811.2:g.13290A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5186A>T
ENST00000482662.2:n.3593A>T
ENST00000685865.1:n.1545A>T
ENST00000687250.1:n.1245A>T
ENST00000687995.1:n.1494A>T
ENST00000688205.1:c.*735A>T	ENSP00000509673.1:n.*735A>T
ENST00000688788.1:n.1381A>T
ENST00000689276.1:c.1073A>T	ENSP00000510012.1:p.His358Leu
ENST00000689576.1:c.1142A>T	ENSP00000508712.1:p.His381Leu
ENST00000690108.1:c.*798A>T	ENSP00000510617.1:n.*798A>T
ENST00000690468.1:c.863A>T	ENSP00000509078.1:p.His288Leu
ENST00000690595.1:c.467A>T	ENSP00000508979.1:p.His156Leu
ENST00000691348.1:c.971A>T	ENSP00000509369.1:p.His324Leu
ENST00000691410.1:c.*719A>T	ENSP00000508479.1:n.*719A>T
ENST00000693287.1:c.458A>T	ENSP00000510264.1:p.His153Leu
ENST00000693681.1:c.455A>T	ENSP00000510789.1:p.His152Leu
ENST00000233838.9:c.1142A>T MANE Select	ENSP00000233838.3:p.His381Leu
ENST00000233838.8:c.1142A>T	ENSP00000233838.3:p.His381Leu
ENST00000430215.7:c.971A>T	ENSP00000408045.3:p.His324Leu
ENST00000465637.5:n.179-5241A>T
ENST00000473665.1:n.635A>T
ENST00000482662.1:n.559A>T
NM_000821.5:c.1142A>T	NP_000812.2:p.His381Leu
NM_000821.6:c.1142A>T	NP_000812.2:p.His381Leu
NM_001142269.2:c.971A>T	NP_001135741.1:p.His324Leu
NM_001142269.3:c.971A>T	NP_001135741.1:p.His324Leu
XM_005264259.3:c.1142A>T	XP_005264316.1:p.His381Leu
XM_011532764.1:c.320A>T	XP_011531066.1:p.His107Leu
XM_011532765.1:c.320A>T	XP_011531067.1:p.His107Leu
XR_939677.1:n.1207A>T
XM_005264259.5:c.1142A>T	XP_005264316.1:p.His381Leu
XM_011532764.3:c.320A>T	XP_011531066.1:p.His107Leu
XM_011532765.3:c.320A>T	XP_011531067.1:p.His107Leu
XM_017003803.2:c.971A>T	XP_016859292.1:p.His324Leu
XR_001738703.2:n.1207A>T
NM_000821.7:c.1142A>T MANE Select	NP_000812.2:p.His381Leu
NM_001142269.4:c.971A>T	NP_001135741.1:p.His324Leu