Canonical Allele Identifier: CA3860056

Gene: GCLC GCLC-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.53500356G>A , CM000668.2:g.53500356G>A	GRCh38
NC_000006.11:g.53365154G>A , CM000668.1:g.53365154G>A	GRCh37
NC_000006.10:g.53473113G>A	NCBI36
NG_012071.1:g.49678C>T
NG_012071.2:g.49774C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513939.6:c.1364-6C>T (GCLC)	ENSP00000424211.2:n.1364-6C>T
ENST00000616923.5:c.1319-6C>T (GCLC)	ENSP00000482756.2:n.1319-6C>T
ENST00000643939.1:c.1484-6C>T (GCLC)	ENSP00000495686.1:n.1484-6C>T
ENST00000650454.1:c.1478-6C>T (GCLC) MANE Select	ENSP00000497574.1:n.1478-6C>T
ENST00000229416.10:c.1478-6C>T (GCLC)	ENSP00000229416.6:n.1478-6C>T
ENST00000504353.1:n.447-6C>T (GCLC)
ENST00000509541.5:n.1923-6C>T (GCLC)
ENST00000510837.5:n.356-6C>T (GCLC)
ENST00000515580.1:n.995C>T (GCLC)
ENST00000616923.4:c.1364-6C>T (GCLC)	ENSP00000482756.1:n.1364-6C>T
NM_001197115.1:c.1364-6C>T (GCLC)	NP_001184044.1:n.1364-6C>T
NM_001498.3:c.1478-6C>T (GCLC)	NP_001489.1:n.1478-6C>T
XR_926888.1:n.87-5798G>A (GCLC-AS1)
XR_926889.1:n.56-5798G>A (GCLC-AS1)
NM_001498.4:c.1478-6C>T (GCLC) MANE Select	NP_001489.1:n.1478-6C>T
XM_017010749.1:c.767-6C>T (GCLC)	XP_016866238.1:n.767-6C>T
NM_001197115.2:c.1364-6C>T (GCLC)	NP_001184044.1:n.1364-6C>T