Canonical Allele Identifier: CA347492053

Gene: GGCX

Linked Data

• MyVariant Identifiers: chr2:g.85786068C>A (hg19) ; chr2:g.85558945C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85558945C>A , CM000664.2:g.85558945C>A	GRCh38
NC_000002.11:g.85786068C>A , CM000664.1:g.85786068C>A	GRCh37
NC_000002.10:g.85639579C>A	NCBI36
NG_011811.2:g.7590G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.131G>T
ENST00000482662.2:n.411+1G>T
ENST00000496962.2:c.345G>T	ENSP00000508856.1:p.Met115Ile
ENST00000685865.1:n.437G>T
ENST00000687250.1:n.448G>T
ENST00000687995.1:n.386G>T
ENST00000688205.1:c.345G>T	ENSP00000509673.1:p.Met115Ile
ENST00000688788.1:n.437G>T
ENST00000689276.1:c.344+1G>T	ENSP00000510012.1:n.344+1G>T
ENST00000689576.1:c.345G>T	ENSP00000508712.1:p.Met115Ile
ENST00000690108.1:c.344+1G>T	ENSP00000510617.1:n.344+1G>T
ENST00000690468.1:c.173+1G>T	ENSP00000509078.1:n.173+1G>T
ENST00000690595.1:c.214+1870G>T	ENSP00000508979.1:n.214+1870G>T
ENST00000691348.1:c.174G>T	ENSP00000509369.1:p.Met58Ile
ENST00000691410.1:c.344+1G>T	ENSP00000508479.1:n.344+1G>T
ENST00000693287.1:c.-67+2441G>T	ENSP00000510264.1:n.-67+2441G>T
ENST00000693681.1:c.174G>T	ENSP00000510789.1:p.Met58Ile
ENST00000233838.9:c.345G>T MANE Select	ENSP00000233838.3:p.Met115Ile
ENST00000233838.8:c.345G>T	ENSP00000233838.3:p.Met115Ile
ENST00000421496.5:c.173+1G>T	ENSP00000400384.1:n.173+1G>T
ENST00000423570.5:c.344+1G>T	ENSP00000389426.1:n.344+1G>T
ENST00000428479.3:c.174G>T	ENSP00000390748.3:p.Met58Ile
ENST00000430215.7:c.174G>T	ENSP00000408045.3:p.Met58Ile
ENST00000465637.5:n.178+61G>T
ENST00000481541.1:n.239G>T
ENST00000496962.1:n.464G>T
NM_000821.5:c.345G>T	NP_000812.2:p.Met115Ile
NM_000821.6:c.345G>T	NP_000812.2:p.Met115Ile
NM_001142269.2:c.174G>T	NP_001135741.1:p.Met58Ile
NM_001142269.3:c.174G>T	NP_001135741.1:p.Met58Ile
NM_001311312.1:c.345G>T	NP_001298241.1:p.Met115Ile
XM_005264259.3:c.345G>T	XP_005264316.1:p.Met115Ile
XM_011532764.1:c.-314G>T	XP_011531066.1:n.-314G>T
XM_011532765.1:c.-314G>T	XP_011531067.1:n.-314G>T
XR_939677.1:n.410G>T
XM_005264259.5:c.345G>T	XP_005264316.1:p.Met115Ile
XM_011532764.3:c.-314G>T	XP_011531066.1:n.-314G>T
XM_011532765.3:c.-314G>T	XP_011531067.1:n.-314G>T
XM_017003803.2:c.174G>T	XP_016859292.1:p.Met58Ile
XR_001738703.2:n.410G>T
NM_000821.7:c.345G>T MANE Select	NP_000812.2:p.Met115Ile
NM_001142269.4:c.174G>T	NP_001135741.1:p.Met58Ile
NM_001311312.2:c.345G>T	NP_001298241.1:p.Met115Ile