Canonical Allele Identifier: CA1629302487
Gene: GCLC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53506913C= , CM000668.2:g.53506913C= GRCh38
NC_000006.11:g.53371711C= , CM000668.1:g.53371711C= GRCh37
NC_000006.10:g.53479670C= NCBI36
NG_012071.1:g.43121G=
NG_012071.2:g.43217G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000513939.6:c.1083G= ENSP00000424211.2:p.Glu361=
ENST00000616923.5:c.1038G= ENSP00000482756.2:p.Glu346=
ENST00000643939.1:c.1203G= ENSP00000495686.1:p.Glu401=
ENST00000650454.1:c.1197G= MANE Select ENSP00000497574.1:p.Glu399=
ENST00000229416.10:c.1197G= ENSP00000229416.6:p.Glu399=
ENST00000504353.1:n.166G=
ENST00000509541.5:n.1642G=
ENST00000616923.4:c.1083G= ENSP00000482756.1:p.Glu361=
NM_001197115.1:c.1083G= NP_001184044.1:p.Glu361=
NM_001498.3:c.1197G= NP_001489.1:p.Glu399=
NM_001498.4:c.1197G= MANE Select NP_001489.1:p.Glu399=
XM_017010749.1:c.486G= XP_016866238.1:p.Glu162=
NM_001197115.2:c.1083G= NP_001184044.1:p.Glu361=