Canonical Allele Identifier: CA3860356

Gene: GCLC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53516225A>G , CM000668.2:g.53516225A>G	GRCh38
NC_000006.11:g.53381023A>G , CM000668.1:g.53381023A>G	GRCh37
NC_000006.10:g.53488982A>G	NCBI36
NG_012071.1:g.33809T>C
NG_012071.2:g.33905T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.447-1728T>C	ENSP00000424211.2:n.447-1728T>C
ENST00000514933.2:n.378-3T>C
ENST00000616923.5:c.288-3T>C	ENSP00000482756.2:n.288-3T>C
ENST00000643939.1:c.450T>C	ENSP00000495686.1:p.Cys150=
ENST00000650454.1:c.447-3T>C MANE Select	ENSP00000497574.1:n.447-3T>C
ENST00000229416.10:c.447-3T>C	ENSP00000229416.6:n.447-3T>C
ENST00000504525.1:c.151-1693T>C	ENSP00000421228.1:n.151-1693T>C
ENST00000505294.5:c.288-8T>C	ENSP00000421629.1:n.288-8T>C
ENST00000513939.5:c.410-1728T>C
ENST00000514004.5:c.447-3T>C	ENSP00000421908.1:n.447-3T>C
ENST00000514933.1:c.288-3T>C	ENSP00000423615.1:n.288-3T>C
ENST00000616923.4:c.447-1728T>C	ENSP00000482756.1:n.447-1728T>C
NM_001197115.1:c.447-1728T>C	NP_001184044.1:n.447-1728T>C
NM_001498.3:c.447-3T>C	NP_001489.1:n.447-3T>C
NM_001498.4:c.447-3T>C MANE Select	NP_001489.1:n.447-3T>C
XM_017010749.1:c.-300-3T>C	XP_016866238.1:n.-300-3T>C
NM_001197115.2:c.447-1728T>C	NP_001184044.1:n.447-1728T>C