Canonical Allele Identifier: CA347492178
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85558981C>A , CM000664.2:g.85558981C>A GRCh38
NC_000002.11:g.85786104C>A , CM000664.1:g.85786104C>A GRCh37
NC_000002.10:g.85639615C>A NCBI36
NG_011811.2:g.7554G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000473665.2:n.95G>T
ENST00000482662.2:n.376G>T
ENST00000496962.2:c.309G>T ENSP00000508856.1:p.Leu103Phe
ENST00000685865.1:n.401G>T
ENST00000687250.1:n.412G>T
ENST00000687995.1:n.350G>T
ENST00000688205.1:c.309G>T ENSP00000509673.1:p.Leu103Phe
ENST00000688788.1:n.401G>T
ENST00000689276.1:c.309G>T ENSP00000510012.1:p.Leu103Phe
ENST00000689576.1:c.309G>T ENSP00000508712.1:p.Leu103Phe
ENST00000690108.1:c.309G>T ENSP00000510617.1:p.Leu103Phe
ENST00000690468.1:c.138G>T ENSP00000509078.1:p.Leu46Phe
ENST00000690595.1:c.214+1834G>T ENSP00000508979.1:n.214+1834G>T
ENST00000691348.1:c.138G>T ENSP00000509369.1:p.Leu46Phe
ENST00000691410.1:c.309G>T ENSP00000508479.1:p.Leu103Phe
ENST00000693287.1:c.-67+2405G>T ENSP00000510264.1:n.-67+2405G>T
ENST00000693681.1:c.138G>T ENSP00000510789.1:p.Leu46Phe
ENST00000233838.9:c.309G>T MANE Select ENSP00000233838.3:p.Leu103Phe
ENST00000233838.8:c.309G>T ENSP00000233838.3:p.Leu103Phe
ENST00000421496.5:c.138G>T ENSP00000400384.1:p.Leu46Phe
ENST00000423570.5:c.309G>T ENSP00000389426.1:p.Leu103Phe
ENST00000428479.3:c.138G>T ENSP00000390748.3:p.Leu46Phe
ENST00000430215.7:c.138G>T ENSP00000408045.3:p.Leu46Phe
ENST00000465637.5:n.178+25G>T
ENST00000481541.1:n.203G>T
ENST00000496962.1:n.428G>T
NM_000821.5:c.309G>T NP_000812.2:p.Leu103Phe
NM_000821.6:c.309G>T NP_000812.2:p.Leu103Phe
NM_001142269.2:c.138G>T NP_001135741.1:p.Leu46Phe
NM_001142269.3:c.138G>T NP_001135741.1:p.Leu46Phe
NM_001311312.1:c.309G>T NP_001298241.1:p.Leu103Phe
XM_005264259.3:c.309G>T XP_005264316.1:p.Leu103Phe
XM_011532764.1:c.-350G>T XP_011531066.1:n.-350G>T
XM_011532765.1:c.-350G>T XP_011531067.1:n.-350G>T
XR_939677.1:n.374G>T
XM_005264259.5:c.309G>T XP_005264316.1:p.Leu103Phe
XM_011532764.3:c.-350G>T XP_011531066.1:n.-350G>T
XM_011532765.3:c.-350G>T XP_011531067.1:n.-350G>T
XM_017003803.2:c.138G>T XP_016859292.1:p.Leu46Phe
XR_001738703.2:n.374G>T
NM_000821.7:c.309G>T MANE Select NP_000812.2:p.Leu103Phe
NM_001142269.4:c.138G>T NP_001135741.1:p.Leu46Phe
NM_001311312.2:c.309G>T NP_001298241.1:p.Leu103Phe