Canonical Allele Identifier: CA427085164

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780107G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85552984G>T , CM000664.2:g.85552984G>T	GRCh38
NC_000002.11:g.85780107G>T , CM000664.1:g.85780107G>T	GRCh37
NC_000002.10:g.85633618G>T	NCBI36
NG_011811.2:g.13551C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5286C>A
ENST00000482662.2:n.3693C>A
ENST00000685865.1:n.1645C>A
ENST00000687250.1:n.1345C>A
ENST00000687995.1:n.1594C>A
ENST00000688205.1:c.*835C>A	ENSP00000509673.1:n.*835C>A
ENST00000688788.1:n.1481C>A
ENST00000689276.1:c.1173C>A	ENSP00000510012.1:p.Thr391=
ENST00000689576.1:c.1242C>A	ENSP00000508712.1:p.Thr414=
ENST00000690108.1:c.*898C>A	ENSP00000510617.1:n.*898C>A
ENST00000690468.1:c.963C>A	ENSP00000509078.1:p.Thr321=
ENST00000690595.1:c.567C>A	ENSP00000508979.1:p.Thr189=
ENST00000691348.1:c.1071C>A	ENSP00000509369.1:p.Thr357=
ENST00000691410.1:c.*819C>A	ENSP00000508479.1:n.*819C>A
ENST00000693287.1:c.558C>A	ENSP00000510264.1:p.Thr186=
ENST00000693681.1:c.555C>A	ENSP00000510789.1:p.Thr185=
ENST00000233838.9:c.1242C>A MANE Select	ENSP00000233838.3:p.Thr414=
ENST00000233838.8:c.1242C>A	ENSP00000233838.3:p.Thr414=
ENST00000430215.7:c.1071C>A	ENSP00000408045.3:p.Thr357=
ENST00000465637.5:n.179-4980C>A
ENST00000473665.1:n.735C>A
ENST00000482662.1:n.659C>A
NM_000821.5:c.1242C>A	NP_000812.2:p.Thr414=
NM_000821.6:c.1242C>A	NP_000812.2:p.Thr414=
NM_001142269.2:c.1071C>A	NP_001135741.1:p.Thr357=
NM_001142269.3:c.1071C>A	NP_001135741.1:p.Thr357=
XM_005264259.3:c.1242C>A	XP_005264316.1:p.Thr414=
XM_011532764.1:c.420C>A	XP_011531066.1:p.Thr140=
XM_011532765.1:c.420C>A	XP_011531067.1:p.Thr140=
XR_939677.1:n.1307C>A
XM_005264259.5:c.1242C>A	XP_005264316.1:p.Thr414=
XM_011532764.3:c.420C>A	XP_011531066.1:p.Thr140=
XM_011532765.3:c.420C>A	XP_011531067.1:p.Thr140=
XM_017003803.2:c.1071C>A	XP_016859292.1:p.Thr357=
XR_001738703.2:n.1307C>A
NM_000821.7:c.1242C>A MANE Select	NP_000812.2:p.Thr414=
NM_001142269.4:c.1071C>A	NP_001135741.1:p.Thr357=