Canonical Allele Identifier: CA1629302470
Gene: GCLC HGNC NCBI
GCLC-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.53506905_53506906delinsGA , CM000668.2:g.53506905_53506906delinsGA GRCh38
NC_000006.11:g.53371703_53371704delinsGA , CM000668.1:g.53371703_53371704delinsGA GRCh37
NC_000006.10:g.53479662_53479663delinsGA NCBI36
NG_012071.1:g.43128_43129delinsTC
NG_012071.2:g.43224_43225delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000513939.6:c.1083+7_1083+8delinsTC (GCLC) ENSP00000424211.2:n.1083+7_1083+8delinsTC
ENST00000616923.5:c.1038+7_1038+8delinsTC (GCLC) ENSP00000482756.2:n.1038+7_1038+8delinsTC
ENST00000643939.1:c.1203+7_1203+8delinsTC (GCLC) ENSP00000495686.1:n.1203+7_1203+8delinsTC
ENST00000650454.1:c.1197+7_1197+8delinsTC (GCLC) MANE Select ENSP00000497574.1:n.1197+7_1197+8delinsTC
ENST00000229416.10:c.1197+7_1197+8delinsTC (GCLC) ENSP00000229416.6:n.1197+7_1197+8delinsTC
ENST00000504353.1:n.166+7_166+8delinsTC (GCLC)
ENST00000509541.5:n.1642+7_1642+8delinsTC (GCLC)
ENST00000616923.4:c.1083+7_1083+8delinsTC (GCLC) ENSP00000482756.1:n.1083+7_1083+8delinsTC
NM_001197115.1:c.1083+7_1083+8delinsTC (GCLC) NP_001184044.1:n.1083+7_1083+8delinsTC
NM_001498.3:c.1197+7_1197+8delinsTC (GCLC) NP_001489.1:n.1197+7_1197+8delinsTC
XR_926886.1:n.2253_2254delinsGA (GCLC-AS1)
XR_926887.1:n.2247_2248delinsGA (GCLC-AS1)
XR_926888.1:n.475_476delinsGA (GCLC-AS1)
XR_926889.1:n.444_445delinsGA (GCLC-AS1)
NM_001498.4:c.1197+7_1197+8delinsTC (GCLC) MANE Select NP_001489.1:n.1197+7_1197+8delinsTC
XM_017010749.1:c.486+7_486+8delinsTC (GCLC) XP_016866238.1:n.486+7_486+8delinsTC
XR_926886.2:n.579_580delinsGA (GCLC-AS1)
NM_001197115.2:c.1083+7_1083+8delinsTC (GCLC) NP_001184044.1:n.1083+7_1083+8delinsTC