Canonical Allele Identifier: CA3860398

Gene: GCLC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53520971G>T , CM000668.2:g.53520971G>T	GRCh38
NC_000006.11:g.53385769G>T , CM000668.1:g.53385769G>T	GRCh37
NC_000006.10:g.53493728G>T	NCBI36
NG_012071.1:g.29063C>A
NG_012071.2:g.29159C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.264-11C>A	ENSP00000424211.2:n.264-11C>A
ENST00000514933.2:n.195-11C>A
ENST00000616923.5:c.105-11C>A	ENSP00000482756.2:n.105-11C>A
ENST00000643939.1:c.252-11C>A	ENSP00000495686.1:n.252-11C>A
ENST00000650454.1:c.264-11C>A MANE Select	ENSP00000497574.1:n.264-11C>A
ENST00000229416.10:c.264-11C>A	ENSP00000229416.6:n.264-11C>A
ENST00000504525.1:c.151-6439C>A	ENSP00000421228.1:n.151-6439C>A
ENST00000505294.5:c.105-11C>A	ENSP00000421629.1:n.105-11C>A
ENST00000513939.5:c.227-11C>A
ENST00000514004.5:c.264-11C>A	ENSP00000421908.1:n.264-11C>A
ENST00000514933.1:c.105-11C>A	ENSP00000423615.1:n.105-11C>A
ENST00000616923.4:c.264-11C>A	ENSP00000482756.1:n.264-11C>A
NM_001197115.1:c.264-11C>A	NP_001184044.1:n.264-11C>A
NM_001498.3:c.264-11C>A	NP_001489.1:n.264-11C>A
NM_001498.4:c.264-11C>A MANE Select	NP_001489.1:n.264-11C>A
XM_017010749.1:c.-483-11C>A	XP_016866238.1:n.-483-11C>A
NM_001197115.2:c.264-11C>A	NP_001184044.1:n.264-11C>A