Canonical Allele Identifier: CA1629296245

Gene: GCLC

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53527310A>T , CM000668.2:g.53527310A>T	GRCh38
NC_000006.11:g.53392108A>T , CM000668.1:g.53392108A>T	GRCh37
NC_000006.10:g.53500067A>T	NCBI36
NG_012071.1:g.22724T>A
NG_012071.2:g.22820T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.151-4783T>A	ENSP00000424211.2:n.151-4783T>A
ENST00000616923.5:c.-9-4783T>A	ENSP00000482756.2:n.-9-4783T>A
ENST00000643939.1:c.139-4783T>A	ENSP00000495686.1:n.139-4783T>A
ENST00000650454.1:c.151-4783T>A MANE Select	ENSP00000497574.1:n.151-4783T>A
ENST00000229416.10:c.151-4783T>A	ENSP00000229416.6:n.151-4783T>A
ENST00000504525.1:c.151-12778T>A	ENSP00000421228.1:n.151-12778T>A
ENST00000505197.1:c.-9-4783T>A	ENSP00000427403.1:n.-9-4783T>A
ENST00000513939.5:c.114-4783T>A
ENST00000514004.5:c.151-4783T>A	ENSP00000421908.1:n.151-4783T>A
ENST00000616923.4:c.151-4783T>A	ENSP00000482756.1:n.151-4783T>A
NM_001197115.1:c.151-4783T>A	NP_001184044.1:n.151-4783T>A
NM_001498.3:c.151-4783T>A	NP_001489.1:n.151-4783T>A
NM_001498.4:c.151-4783T>A MANE Select	NP_001489.1:n.151-4783T>A
XM_017010749.1:c.-596-4783T>A	XP_016866238.1:n.-596-4783T>A
NM_001197115.2:c.151-4783T>A	NP_001184044.1:n.151-4783T>A