Canonical Allele Identifier: CA347485017

Gene: GGCX

Linked Data

• dbSNP Id: rs1691974681
• MyVariant Identifiers: chr2:g.85779072G>A (hg19) ; chr2:g.85551949G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85551949G>A , CM000664.2:g.85551949G>A	GRCh38
NC_000002.11:g.85779072G>A , CM000664.1:g.85779072G>A	GRCh37
NC_000002.10:g.85632583G>A	NCBI36
NG_011811.2:g.14586C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5950C>T
ENST00000482662.2:n.4357C>T
ENST00000685865.1:n.2309C>T
ENST00000687250.1:n.2009C>T
ENST00000687995.1:n.1824C>T
ENST00000688205.1:c.*1065C>T	ENSP00000509673.1:n.*1065C>T
ENST00000688788.1:n.1711C>T
ENST00000689276.1:c.1403C>T	ENSP00000510012.1:p.Ala468Val
ENST00000689576.1:c.*91C>T	ENSP00000508712.1:n.*91C>T
ENST00000690108.1:c.*1128C>T	ENSP00000510617.1:n.*1128C>T
ENST00000690468.1:c.*24C>T	ENSP00000509078.1:n.*24C>T
ENST00000690595.1:c.797C>T	ENSP00000508979.1:p.Ala266Val
ENST00000691348.1:c.*24C>T	ENSP00000509369.1:n.*24C>T
ENST00000691410.1:c.*1049C>T	ENSP00000508479.1:n.*1049C>T
ENST00000693287.1:c.788C>T	ENSP00000510264.1:p.Ala263Val
ENST00000693681.1:c.785C>T	ENSP00000510789.1:p.Ala262Val
ENST00000233838.9:c.1472C>T MANE Select	ENSP00000233838.3:p.Ala491Val
ENST00000233838.8:c.1472C>T	ENSP00000233838.3:p.Ala491Val
ENST00000430215.7:c.1301C>T	ENSP00000408045.3:p.Ala434Val
ENST00000465637.5:n.179-3945C>T
NM_000821.5:c.1472C>T	NP_000812.2:p.Ala491Val
NM_000821.6:c.1472C>T	NP_000812.2:p.Ala491Val
NM_001142269.2:c.1301C>T	NP_001135741.1:p.Ala434Val
NM_001142269.3:c.1301C>T	NP_001135741.1:p.Ala434Val
XM_005264259.3:c.1472C>T	XP_005264316.1:p.Ala491Val
XM_011532764.1:c.650C>T	XP_011531066.1:p.Ala217Val
XM_011532765.1:c.650C>T	XP_011531067.1:p.Ala217Val
XR_939677.1:n.1385C>T
XM_005264259.5:c.1472C>T	XP_005264316.1:p.Ala491Val
XM_011532764.3:c.650C>T	XP_011531066.1:p.Ala217Val
XM_011532765.3:c.650C>T	XP_011531067.1:p.Ala217Val
XM_017003803.2:c.1301C>T	XP_016859292.1:p.Ala434Val
XR_001738703.2:n.1385C>T
NM_000821.7:c.1472C>T MANE Select	NP_000812.2:p.Ala491Val
NM_001142269.4:c.1301C>T	NP_001135741.1:p.Ala434Val