Canonical Allele Identifier: CA3860039

Gene: GCLC GCLC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53500304C>T , CM000668.2:g.53500304C>T	GRCh38
NC_000006.11:g.53365102C>T , CM000668.1:g.53365102C>T	GRCh37
NC_000006.10:g.53473061C>T	NCBI36
NG_012071.1:g.49730G>A
NG_012071.2:g.49826G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.1410G>A (GCLC)	ENSP00000424211.2:p.Thr470=
ENST00000616923.5:c.1365G>A (GCLC)	ENSP00000482756.2:p.Thr455=
ENST00000643939.1:c.1530G>A (GCLC)	ENSP00000495686.1:p.Thr510=
ENST00000650454.1:c.1524G>A (GCLC) MANE Select	ENSP00000497574.1:p.Thr508=
ENST00000229416.10:c.1524G>A (GCLC)	ENSP00000229416.6:p.Thr508=
ENST00000504353.1:n.493G>A (GCLC)
ENST00000509541.5:n.1969G>A (GCLC)
ENST00000510837.5:n.402G>A (GCLC)
ENST00000515580.1:n.1047G>A (GCLC)
ENST00000616923.4:c.1410G>A (GCLC)	ENSP00000482756.1:p.Thr470=
NM_001197115.1:c.1410G>A (GCLC)	NP_001184044.1:p.Thr470=
NM_001498.3:c.1524G>A (GCLC)	NP_001489.1:p.Thr508=
XR_926888.1:n.87-5850C>T (GCLC-AS1)
XR_926889.1:n.56-5850C>T (GCLC-AS1)
NM_001498.4:c.1524G>A (GCLC) MANE Select	NP_001489.1:p.Thr508=
XM_017010749.1:c.813G>A (GCLC)	XP_016866238.1:p.Thr271=
NM_001197115.2:c.1410G>A (GCLC)	NP_001184044.1:p.Thr470=