Canonical Allele Identifier: CA361849627
Gene: GLRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151822705T>A , CM000667.2:g.151822705T>A GRCh38
NC_000005.9:g.151202266T>A , CM000667.1:g.151202266T>A GRCh37
NC_000005.8:g.151182459T>A NCBI36
NG_011764.1:g.107132A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1318A>T MANE Select ENSP00000274576.5:p.Ile440Phe
ENST00000274576.8:c.1318A>T ENSP00000274576.4:p.Ile440Phe
ENST00000455880.2:c.1342A>T ENSP00000411593.2:p.Ile448Phe
ENST00000462581.6:c.*1076A>T ENSP00000430595.1:n.*1076A>T
NM_000171.3:c.1318A>T NP_000162.2:p.Ile440Phe
NM_001146040.1:c.1342A>T NP_001139512.1:p.Ile448Phe
NM_001292000.1:c.1069A>T NP_001278929.1:p.Ile357Phe
NM_000171.4:c.1318A>T MANE Select NP_000162.2:p.Ile440Phe
NM_001146040.2:c.1342A>T NP_001139512.1:p.Ile448Phe
NM_001292000.2:c.1069A>T NP_001278929.1:p.Ile357Phe