Canonical Allele Identifier: CA347492387
Gene: GGCX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85559036A>G , CM000664.2:g.85559036A>G GRCh38
NC_000002.11:g.85786159A>G , CM000664.1:g.85786159A>G GRCh37
NC_000002.10:g.85639670A>G NCBI36
NG_011811.2:g.7499T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.40T>C
ENST00000482662.2:n.321T>C
ENST00000496962.2:c.254T>C ENSP00000508856.1:p.Leu85Pro
ENST00000685865.1:n.346T>C
ENST00000687250.1:n.357T>C
ENST00000687995.1:n.295T>C
ENST00000688205.1:c.254T>C ENSP00000509673.1:p.Leu85Pro
ENST00000688788.1:n.346T>C
ENST00000689276.1:c.254T>C ENSP00000510012.1:p.Leu85Pro
ENST00000689576.1:c.254T>C ENSP00000508712.1:p.Leu85Pro
ENST00000690108.1:c.254T>C ENSP00000510617.1:p.Leu85Pro
ENST00000690468.1:c.83T>C ENSP00000509078.1:p.Leu28Pro
ENST00000690595.1:c.214+1779T>C ENSP00000508979.1:n.214+1779T>C
ENST00000691348.1:c.83T>C ENSP00000509369.1:p.Leu28Pro
ENST00000691410.1:c.254T>C ENSP00000508479.1:p.Leu85Pro
ENST00000693287.1:c.-67+2350T>C ENSP00000510264.1:n.-67+2350T>C
ENST00000693681.1:c.83T>C ENSP00000510789.1:p.Leu28Pro
ENST00000233838.9:c.254T>C MANE Select ENSP00000233838.3:p.Leu85Pro
ENST00000233838.8:c.254T>C ENSP00000233838.3:p.Leu85Pro
ENST00000421496.5:c.83T>C ENSP00000400384.1:p.Leu28Pro
ENST00000423570.5:c.254T>C ENSP00000389426.1:p.Leu85Pro
ENST00000428479.3:c.83T>C ENSP00000390748.3:p.Leu28Pro
ENST00000430215.7:c.83T>C ENSP00000408045.3:p.Leu28Pro
ENST00000465637.5:n.148T>C
ENST00000481541.1:n.148T>C
ENST00000496962.1:n.373T>C
NM_000821.5:c.254T>C NP_000812.2:p.Leu85Pro
NM_000821.6:c.254T>C NP_000812.2:p.Leu85Pro
NM_001142269.2:c.83T>C NP_001135741.1:p.Leu28Pro
NM_001142269.3:c.83T>C NP_001135741.1:p.Leu28Pro
NM_001311312.1:c.254T>C NP_001298241.1:p.Leu85Pro
XM_005264259.3:c.254T>C XP_005264316.1:p.Leu85Pro
XM_011532764.1:c.-405T>C XP_011531066.1:n.-405T>C
XM_011532765.1:c.-405T>C XP_011531067.1:n.-405T>C
XR_939677.1:n.319T>C
XM_005264259.5:c.254T>C XP_005264316.1:p.Leu85Pro
XM_011532764.3:c.-405T>C XP_011531066.1:n.-405T>C
XM_011532765.3:c.-405T>C XP_011531067.1:n.-405T>C
XM_017003803.2:c.83T>C XP_016859292.1:p.Leu28Pro
XR_001738703.2:n.319T>C
NM_000821.7:c.254T>C MANE Select NP_000812.2:p.Leu85Pro
NM_001142269.4:c.83T>C NP_001135741.1:p.Leu28Pro
NM_001311312.2:c.254T>C NP_001298241.1:p.Leu85Pro