Canonical Allele Identifier: CA1591568017
Gene: GLRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151829040_151829046delinsAAATGTC , CM000667.2:g.151829040_151829046delinsAAATGTC GRCh38
NC_000005.9:g.151208601_151208607delinsAAATGTC , CM000667.1:g.151208601_151208607delinsAAATGTC GRCh37
NC_000005.8:g.151188794_151188800delinsAAATGTC NCBI36
NG_011764.1:g.100791_100797delinsGACATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.934_940delinsGACATTT MANE Select ENSP00000274576.5:p.Asp312=
ENST00000274576.8:c.934_940delinsGACATTT ENSP00000274576.4:p.Asp312=
ENST00000455880.2:c.934_940delinsGACATTT ENSP00000411593.2:p.Asp312=
ENST00000462581.6:c.*692_*698delinsGACATTT ENSP00000430595.1:n.*692_*698delinsGACATTT
NM_000171.3:c.934_940delinsGACATTT NP_000162.2:p.Asp312=
NM_001146040.1:c.934_940delinsGACATTT NP_001139512.1:p.Asp312=
NM_001292000.1:c.685_691delinsGACATTT NP_001278929.1:p.Asp229=
NM_000171.4:c.934_940delinsGACATTT MANE Select NP_000162.2:p.Asp312=
NM_001146040.2:c.934_940delinsGACATTT NP_001139512.1:p.Asp312=
NM_001292000.2:c.685_691delinsGACATTT NP_001278929.1:p.Asp229=