Canonical Allele Identifier: CA364471314

Gene: GCLC GCLC-AS1

Linked Data

• MyVariant Identifiers: chr6:g.53371709A>C (hg19) ; chr6:g.53506911A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53506911A>C , CM000668.2:g.53506911A>C	GRCh38
NC_000006.11:g.53371709A>C , CM000668.1:g.53371709A>C	GRCh37
NC_000006.10:g.53479668A>C	NCBI36
NG_012071.1:g.43123T>G
NG_012071.2:g.43219T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.1083+2T>G (GCLC)	ENSP00000424211.2:n.1083+2T>G
ENST00000616923.5:c.1038+2T>G (GCLC)	ENSP00000482756.2:n.1038+2T>G
ENST00000643939.1:c.1203+2T>G (GCLC)	ENSP00000495686.1:n.1203+2T>G
ENST00000650454.1:c.1197+2T>G (GCLC) MANE Select	ENSP00000497574.1:n.1197+2T>G
ENST00000229416.10:c.1197+2T>G (GCLC)	ENSP00000229416.6:n.1197+2T>G
ENST00000504353.1:n.166+2T>G (GCLC)
ENST00000509541.5:n.1642+2T>G (GCLC)
ENST00000616923.4:c.1083+2T>G (GCLC)	ENSP00000482756.1:n.1083+2T>G
NM_001197115.1:c.1083+2T>G (GCLC)	NP_001184044.1:n.1083+2T>G
NM_001498.3:c.1197+2T>G (GCLC)	NP_001489.1:n.1197+2T>G
XR_926886.1:n.2259A>C (GCLC-AS1)
XR_926887.1:n.2253A>C (GCLC-AS1)
XR_926888.1:n.481A>C (GCLC-AS1)
XR_926889.1:n.450A>C (GCLC-AS1)
NM_001498.4:c.1197+2T>G (GCLC) MANE Select	NP_001489.1:n.1197+2T>G
XM_017010749.1:c.486+2T>G (GCLC)	XP_016866238.1:n.486+2T>G
XR_926886.2:n.585A>C (GCLC-AS1)
NM_001197115.2:c.1083+2T>G (GCLC)	NP_001184044.1:n.1083+2T>G