Canonical Allele Identifier: CA3523461
Gene: GLRA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1444286
ClinVar RCV Id: RCV001955867
dbSNP Id: rs555222589
ExAC: 5:151202265 A / G
gnomAD v2: 5-151202265-A-G
gnomAD v3: 5-151822704-A-G
gnomAD v4: 5-151822704-A-G
MyVariant Identifiers: chr5:g.151202265A>G (hg19) chr5:g.151822704A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151822704A>G , CM000667.2:g.151822704A>G GRCh38
NC_000005.9:g.151202265A>G , CM000667.1:g.151202265A>G GRCh37
NC_000005.8:g.151182458A>G NCBI36
NG_011764.1:g.107133T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1319T>C MANE Select ENSP00000274576.5:p.Ile440Thr
ENST00000274576.8:c.1319T>C ENSP00000274576.4:p.Ile440Thr
ENST00000455880.2:c.1343T>C ENSP00000411593.2:p.Ile448Thr
ENST00000462581.6:c.*1077T>C ENSP00000430595.1:n.*1077T>C
NM_000171.3:c.1319T>C NP_000162.2:p.Ile440Thr
NM_001146040.1:c.1343T>C NP_001139512.1:p.Ile448Thr
NM_001292000.1:c.1070T>C NP_001278929.1:p.Ile357Thr
NM_000171.4:c.1319T>C MANE Select NP_000162.2:p.Ile440Thr
NM_001146040.2:c.1343T>C NP_001139512.1:p.Ile448Thr
NM_001292000.2:c.1070T>C NP_001278929.1:p.Ile357Thr
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