Canonical Allele Identifier: CA447226601

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151202399A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822838A>T , CM000667.2:g.151822838A>T	GRCh38
NC_000005.9:g.151202399A>T , CM000667.1:g.151202399A>T	GRCh37
NC_000005.8:g.151182592A>T	NCBI36
NG_011764.1:g.106999T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1185T>A MANE Select	ENSP00000274576.5:p.Pro395=
ENST00000274576.8:c.1185T>A	ENSP00000274576.4:p.Pro395=
ENST00000455880.2:c.1209T>A	ENSP00000411593.2:p.Pro403=
ENST00000462581.6:c.*943T>A	ENSP00000430595.1:n.*943T>A
NM_000171.3:c.1185T>A	NP_000162.2:p.Pro395=
NM_001146040.1:c.1209T>A	NP_001139512.1:p.Pro403=
NM_001292000.1:c.936T>A	NP_001278929.1:p.Pro312=
NM_000171.4:c.1185T>A MANE Select	NP_000162.2:p.Pro395=
NM_001146040.2:c.1209T>A	NP_001139512.1:p.Pro403=
NM_001292000.2:c.936T>A	NP_001278929.1:p.Pro312=