Canonical Allele Identifier: CA447226748
Gene: GLRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.151208532G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151828971G>T , CM000667.2:g.151828971G>T GRCh38
NC_000005.9:g.151208532G>T , CM000667.1:g.151208532G>T GRCh37
NC_000005.8:g.151188725G>T NCBI36
NG_011764.1:g.100866C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1009C>A MANE Select ENSP00000274576.5:p.Arg337=
ENST00000274576.8:c.1009C>A ENSP00000274576.4:p.Arg337=
ENST00000455880.2:c.1009C>A ENSP00000411593.2:p.Arg337=
ENST00000462581.6:c.*767C>A ENSP00000430595.1:n.*767C>A
NM_000171.3:c.1009C>A NP_000162.2:p.Arg337=
NM_001146040.1:c.1009C>A NP_001139512.1:p.Arg337=
NM_001292000.1:c.760C>A NP_001278929.1:p.Arg254=
NM_000171.4:c.1009C>A MANE Select NP_000162.2:p.Arg337=
NM_001146040.2:c.1009C>A NP_001139512.1:p.Arg337=
NM_001292000.2:c.760C>A NP_001278929.1:p.Arg254=