Canonical Allele Identifier: CA347487358

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780377G>C (hg19) ; chr2:g.85553254G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553254G>C , CM000664.2:g.85553254G>C	GRCh38
NC_000002.11:g.85780377G>C , CM000664.1:g.85780377G>C	GRCh37
NC_000002.10:g.85633888G>C	NCBI36
NG_011811.2:g.13281C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5177C>G
ENST00000482662.2:n.3584C>G
ENST00000685865.1:n.1536C>G
ENST00000687250.1:n.1236C>G
ENST00000687995.1:n.1485C>G
ENST00000688205.1:c.*726C>G	ENSP00000509673.1:n.*726C>G
ENST00000688788.1:n.1372C>G
ENST00000689276.1:c.1064C>G	ENSP00000510012.1:p.Pro355Arg
ENST00000689576.1:c.1133C>G	ENSP00000508712.1:p.Pro378Arg
ENST00000690108.1:c.*789C>G	ENSP00000510617.1:n.*789C>G
ENST00000690468.1:c.854C>G	ENSP00000509078.1:p.Pro285Arg
ENST00000690595.1:c.458C>G	ENSP00000508979.1:p.Pro153Arg
ENST00000691348.1:c.962C>G	ENSP00000509369.1:p.Pro321Arg
ENST00000691410.1:c.*710C>G	ENSP00000508479.1:n.*710C>G
ENST00000693287.1:c.449C>G	ENSP00000510264.1:p.Pro150Arg
ENST00000693681.1:c.446C>G	ENSP00000510789.1:p.Pro149Arg
ENST00000233838.9:c.1133C>G MANE Select	ENSP00000233838.3:p.Pro378Arg
ENST00000233838.8:c.1133C>G	ENSP00000233838.3:p.Pro378Arg
ENST00000430215.7:c.962C>G	ENSP00000408045.3:p.Pro321Arg
ENST00000465637.5:n.179-5250C>G
ENST00000473665.1:n.626C>G
ENST00000482662.1:n.550C>G
NM_000821.5:c.1133C>G	NP_000812.2:p.Pro378Arg
NM_000821.6:c.1133C>G	NP_000812.2:p.Pro378Arg
NM_001142269.2:c.962C>G	NP_001135741.1:p.Pro321Arg
NM_001142269.3:c.962C>G	NP_001135741.1:p.Pro321Arg
XM_005264259.3:c.1133C>G	XP_005264316.1:p.Pro378Arg
XM_011532764.1:c.311C>G	XP_011531066.1:p.Pro104Arg
XM_011532765.1:c.311C>G	XP_011531067.1:p.Pro104Arg
XR_939677.1:n.1198C>G
XM_005264259.5:c.1133C>G	XP_005264316.1:p.Pro378Arg
XM_011532764.3:c.311C>G	XP_011531066.1:p.Pro104Arg
XM_011532765.3:c.311C>G	XP_011531067.1:p.Pro104Arg
XM_017003803.2:c.962C>G	XP_016859292.1:p.Pro321Arg
XR_001738703.2:n.1198C>G
NM_000821.7:c.1133C>G MANE Select	NP_000812.2:p.Pro378Arg
NM_001142269.4:c.962C>G	NP_001135741.1:p.Pro321Arg