Canonical Allele Identifier: CA347486985

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85780136A>G (hg19) ; chr2:g.85553013A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553013A>G , CM000664.2:g.85553013A>G	GRCh38
NC_000002.11:g.85780136A>G , CM000664.1:g.85780136A>G	GRCh37
NC_000002.10:g.85633647A>G	NCBI36
NG_011811.2:g.13522T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5257T>C
ENST00000482662.2:n.3664T>C
ENST00000685865.1:n.1616T>C
ENST00000687250.1:n.1316T>C
ENST00000687995.1:n.1565T>C
ENST00000688205.1:c.*806T>C	ENSP00000509673.1:n.*806T>C
ENST00000688788.1:n.1452T>C
ENST00000689276.1:c.1144T>C	ENSP00000510012.1:p.Ser382Pro
ENST00000689576.1:c.1213T>C	ENSP00000508712.1:p.Ser405Pro
ENST00000690108.1:c.*869T>C	ENSP00000510617.1:n.*869T>C
ENST00000690468.1:c.934T>C	ENSP00000509078.1:p.Ser312Pro
ENST00000690595.1:c.538T>C	ENSP00000508979.1:p.Ser180Pro
ENST00000691348.1:c.1042T>C	ENSP00000509369.1:p.Ser348Pro
ENST00000691410.1:c.*790T>C	ENSP00000508479.1:n.*790T>C
ENST00000693287.1:c.529T>C	ENSP00000510264.1:p.Ser177Pro
ENST00000693681.1:c.526T>C	ENSP00000510789.1:p.Ser176Pro
ENST00000233838.9:c.1213T>C MANE Select	ENSP00000233838.3:p.Ser405Pro
ENST00000233838.8:c.1213T>C	ENSP00000233838.3:p.Ser405Pro
ENST00000430215.7:c.1042T>C	ENSP00000408045.3:p.Ser348Pro
ENST00000465637.5:n.179-5009T>C
ENST00000473665.1:n.706T>C
ENST00000482662.1:n.630T>C
NM_000821.5:c.1213T>C	NP_000812.2:p.Ser405Pro
NM_000821.6:c.1213T>C	NP_000812.2:p.Ser405Pro
NM_001142269.2:c.1042T>C	NP_001135741.1:p.Ser348Pro
NM_001142269.3:c.1042T>C	NP_001135741.1:p.Ser348Pro
XM_005264259.3:c.1213T>C	XP_005264316.1:p.Ser405Pro
XM_011532764.1:c.391T>C	XP_011531066.1:p.Ser131Pro
XM_011532765.1:c.391T>C	XP_011531067.1:p.Ser131Pro
XR_939677.1:n.1278T>C
XM_005264259.5:c.1213T>C	XP_005264316.1:p.Ser405Pro
XM_011532764.3:c.391T>C	XP_011531066.1:p.Ser131Pro
XM_011532765.3:c.391T>C	XP_011531067.1:p.Ser131Pro
XM_017003803.2:c.1042T>C	XP_016859292.1:p.Ser348Pro
XR_001738703.2:n.1278T>C
NM_000821.7:c.1213T>C MANE Select	NP_000812.2:p.Ser405Pro
NM_001142269.4:c.1042T>C	NP_001135741.1:p.Ser348Pro