Canonical Allele Identifier: CA447420351
Gene: GLRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.151239357G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151859796G>A , CM000667.2:g.151859796G>A GRCh38
NC_000005.9:g.151239357G>A , CM000667.1:g.151239357G>A GRCh37
NC_000005.8:g.151219550G>A NCBI36
NG_011764.1:g.70041C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000274576.9:c.465C>T MANE Select ENSP00000274576.5:p.Leu155=
ENST00000274576.8:c.465C>T ENSP00000274576.4:p.Leu155=
ENST00000455880.2:c.465C>T ENSP00000411593.2:p.Leu155=
ENST00000462581.6:c.*223C>T ENSP00000430595.1:n.*223C>T
ENST00000471351.2:n.748C>T
NM_000171.3:c.465C>T NP_000162.2:p.Leu155=
NM_001146040.1:c.465C>T NP_001139512.1:p.Leu155=
NM_001292000.1:c.216C>T NP_001278929.1:p.Leu72=
XM_005268412.2:c.465C>T XP_005268469.1:p.Leu155=
XR_002956230.1:n.229+1903G>A
NM_000171.4:c.465C>T MANE Select NP_000162.2:p.Leu155=
NM_001146040.2:c.465C>T NP_001139512.1:p.Leu155=
NM_001292000.2:c.216C>T NP_001278929.1:p.Leu72=