Canonical Allele Identifier: CA3860101
Gene: GCLC HGNC NCBI
GCLC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53505403G>A , CM000668.2:g.53505403G>A GRCh38
NC_000006.11:g.53370201G>A , CM000668.1:g.53370201G>A GRCh37
NC_000006.10:g.53478160G>A NCBI36
NG_012071.1:g.44631C>T
NG_012071.2:g.44727C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000513939.6:c.1270C>T (GCLC) ENSP00000424211.2:p.Pro424Ser
ENST00000514373.3:n.190C>T (GCLC)
ENST00000616923.5:c.1225C>T (GCLC) ENSP00000482756.2:p.Pro409Ser
ENST00000643939.1:c.1390C>T (GCLC) ENSP00000495686.1:p.Pro464Ser
ENST00000650454.1:c.1384C>T (GCLC) MANE Select ENSP00000497574.1:p.Pro462Ser
ENST00000229416.10:c.1384C>T (GCLC) ENSP00000229416.6:p.Pro462Ser
ENST00000504353.1:n.353C>T (GCLC)
ENST00000509541.5:n.1829C>T (GCLC)
ENST00000510837.5:n.262C>T (GCLC)
ENST00000514373.2:c.187C>T (GCLC) ENSP00000426578.2:p.Pro63Ser
ENST00000616923.4:c.1270C>T (GCLC) ENSP00000482756.1:p.Pro424Ser
NM_001197115.1:c.1270C>T (GCLC) NP_001184044.1:p.Pro424Ser
NM_001498.3:c.1384C>T (GCLC) NP_001489.1:p.Pro462Ser
XR_926886.1:n.1865-751G>A (GCLC-AS1)
XR_926887.1:n.1865-757G>A (GCLC-AS1)
XR_926888.1:n.87-751G>A (GCLC-AS1)
XR_926889.1:n.56-751G>A (GCLC-AS1)
NM_001498.4:c.1384C>T (GCLC) MANE Select NP_001489.1:p.Pro462Ser
XM_017010749.1:c.673C>T (GCLC) XP_016866238.1:p.Pro225Ser
XR_926886.2:n.191-751G>A (GCLC-AS1)
NM_001197115.2:c.1270C>T (GCLC) NP_001184044.1:p.Pro424Ser