Canonical Allele Identifier: CA1629302481

Gene: GCLC GCLC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53506910T= , CM000668.2:g.53506910T=	GRCh38
NC_000006.11:g.53371708T= , CM000668.1:g.53371708T=	GRCh37
NC_000006.10:g.53479667T=	NCBI36
NG_012071.1:g.43124A=
NG_012071.2:g.43220A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.1083+3A= (GCLC)	ENSP00000424211.2:n.1083+3A=
ENST00000616923.5:c.1038+3A= (GCLC)	ENSP00000482756.2:n.1038+3A=
ENST00000643939.1:c.1203+3A= (GCLC)	ENSP00000495686.1:n.1203+3A=
ENST00000650454.1:c.1197+3A= (GCLC) MANE Select	ENSP00000497574.1:n.1197+3A=
ENST00000229416.10:c.1197+3A= (GCLC)	ENSP00000229416.6:n.1197+3A=
ENST00000504353.1:n.166+3A= (GCLC)
ENST00000509541.5:n.1642+3A= (GCLC)
ENST00000616923.4:c.1083+3A= (GCLC)	ENSP00000482756.1:n.1083+3A=
NM_001197115.1:c.1083+3A= (GCLC)	NP_001184044.1:n.1083+3A=
NM_001498.3:c.1197+3A= (GCLC)	NP_001489.1:n.1197+3A=
XR_926886.1:n.2258T= (GCLC-AS1)
XR_926887.1:n.2252T= (GCLC-AS1)
XR_926888.1:n.480T= (GCLC-AS1)
XR_926889.1:n.449T= (GCLC-AS1)
NM_001498.4:c.1197+3A= (GCLC) MANE Select	NP_001489.1:n.1197+3A=
XM_017010749.1:c.486+3A= (GCLC)	XP_016866238.1:n.486+3A=
XR_926886.2:n.584T= (GCLC-AS1)
NM_001197115.2:c.1083+3A= (GCLC)	NP_001184044.1:n.1083+3A=