Canonical Allele Identifier: CA130005965
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs144976473
gnomAD v2: 5-151202127-TGTAA-T
gnomAD v3: 5-151822566-TGTAA-T
gnomAD v4: 5-151822566-TGTAA-T
MyVariant Identifiers: chr5:g.151202128_151202131del (hg19) chr5:g.151822567_151822570del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151822569_151822572del , CM000667.2:g.151822569_151822572del GRCh38
NC_000005.9:g.151202130_151202133del , CM000667.1:g.151202130_151202133del GRCh37
NC_000005.8:g.151182323_151182326del NCBI36
NG_011764.1:g.107267_107270del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.*103_*106del MANE Select ENSP00000274576.5:n.*103_*106del
ENST00000274576.8:c.*103_*106del ENSP00000274576.4:n.*103_*106del
NM_000171.3:c.*103_*106del NP_000162.2:n.*103_*106del
NM_001146040.1:c.*103_*106del NP_001139512.1:n.*103_*106del
NM_001292000.1:c.*103_*106del NP_001278929.1:n.*103_*106del
NM_000171.4:c.*103_*106del MANE Select NP_000162.2:n.*103_*106del
NM_001146040.2:c.*103_*106del NP_001139512.1:n.*103_*106del
NM_001292000.2:c.*103_*106del NP_001278929.1:n.*103_*106del
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