Canonical Allele Identifier: CA447226673
Gene: GLRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.151202501G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151822940G>C , CM000667.2:g.151822940G>C GRCh38
NC_000005.9:g.151202501G>C , CM000667.1:g.151202501G>C GRCh37
NC_000005.8:g.151182694G>C NCBI36
NG_011764.1:g.106897C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1083C>G MANE Select ENSP00000274576.5:p.Arg361=
ENST00000274576.8:c.1083C>G ENSP00000274576.4:p.Arg361=
ENST00000455880.2:c.1107C>G ENSP00000411593.2:p.Arg369=
ENST00000462581.6:c.*841C>G ENSP00000430595.1:n.*841C>G
NM_000171.3:c.1083C>G NP_000162.2:p.Arg361=
NM_001146040.1:c.1107C>G NP_001139512.1:p.Arg369=
NM_001292000.1:c.834C>G NP_001278929.1:p.Arg278=
NM_000171.4:c.1083C>G MANE Select NP_000162.2:p.Arg361=
NM_001146040.2:c.1107C>G NP_001139512.1:p.Arg369=
NM_001292000.2:c.834C>G NP_001278929.1:p.Arg278=