Canonical Allele Identifier: CA447226739

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151208515C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151828954C>A , CM000667.2:g.151828954C>A	GRCh38
NC_000005.9:g.151208515C>A , CM000667.1:g.151208515C>A	GRCh37
NC_000005.8:g.151188708C>A	NCBI36
NG_011764.1:g.100883G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1026G>T MANE Select	ENSP00000274576.5:p.Leu342=
ENST00000274576.8:c.1026G>T	ENSP00000274576.4:p.Leu342=
ENST00000455880.2:c.1026G>T	ENSP00000411593.2:p.Leu342=
ENST00000462581.6:c.*784G>T	ENSP00000430595.1:n.*784G>T
NM_000171.3:c.1026G>T	NP_000162.2:p.Leu342=
NM_001146040.1:c.1026G>T	NP_001139512.1:p.Leu342=
NM_001292000.1:c.777G>T	NP_001278929.1:p.Leu259=
NM_000171.4:c.1026G>T MANE Select	NP_000162.2:p.Leu342=
NM_001146040.2:c.1026G>T	NP_001139512.1:p.Leu342=
NM_001292000.2:c.777G>T	NP_001278929.1:p.Leu259=