Canonical Allele Identifier: CA3038629242

Gene: GCLC GCLC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53505307A>T , CM000668.2:g.53505307A>T	GRCh38
NC_000006.11:g.53370105A>T , CM000668.1:g.53370105A>T	GRCh37
NC_000006.10:g.53478064A>T	NCBI36
NG_012071.1:g.44727T>A
NG_012071.2:g.44823T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001498.4:c.1395+85T>A (GCLC) MANE Select	NP_001489.1:n.1395+85T>A
ENST00000650454.1:c.1395+85T>A (GCLC) MANE Select	ENSP00000497574.1:n.1395+85T>A
NM_001197115.1:c.1281+85T>A (GCLC)	NP_001184044.1:n.1281+85T>A
NM_001197115.2:c.1281+85T>A (GCLC)	NP_001184044.1:n.1281+85T>A
NM_001498.3:c.1395+85T>A (GCLC)	NP_001489.1:n.1395+85T>A
ENST00000229416.10:c.1395+85T>A (GCLC)	ENSP00000229416.6:n.1395+85T>A
ENST00000504353.1:n.364+85T>A (GCLC)
ENST00000509541.5:n.1840+85T>A (GCLC)
ENST00000510837.5:n.273+85T>A (GCLC)
ENST00000513939.6:c.1281+85T>A (GCLC)	ENSP00000424211.2:n.1281+85T>A
ENST00000514373.2:c.283T>A (GCLC)	ENSP00000426578.2:n.283T>A
ENST00000514373.3:n.286T>A (GCLC)
ENST00000616923.4:c.1281+85T>A (GCLC)	ENSP00000482756.1:n.1281+85T>A
ENST00000616923.5:c.1236+85T>A (GCLC)	ENSP00000482756.2:n.1236+85T>A
ENST00000643939.1:c.1401+85T>A (GCLC)	ENSP00000495686.1:n.1401+85T>A
XM_017010749.1:c.684+85T>A (GCLC)	XP_016866238.1:n.684+85T>A
XR_926886.1:n.1865-847A>T (GCLC-AS1)
XR_926886.2:n.191-847A>T (GCLC-AS1)
XR_926887.1:n.1865-853A>T (GCLC-AS1)
XR_926888.1:n.87-847A>T (GCLC-AS1)
XR_926889.1:n.56-847A>T (GCLC-AS1)