Canonical Allele Identifier: CA447226587

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151202381T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822820T>A , CM000667.2:g.151822820T>A	GRCh38
NC_000005.9:g.151202381T>A , CM000667.1:g.151202381T>A	GRCh37
NC_000005.8:g.151182574T>A	NCBI36
NG_011764.1:g.107017A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000274576.9:c.1203A>T MANE Select	ENSP00000274576.5:p.Pro401=
ENST00000274576.8:c.1203A>T	ENSP00000274576.4:p.Pro401=
ENST00000455880.2:c.1227A>T	ENSP00000411593.2:p.Pro409=
ENST00000462581.6:c.*961A>T	ENSP00000430595.1:n.*961A>T
NM_000171.3:c.1203A>T	NP_000162.2:p.Pro401=
NM_001146040.1:c.1227A>T	NP_001139512.1:p.Pro409=
NM_001292000.1:c.954A>T	NP_001278929.1:p.Pro318=
NM_000171.4:c.1203A>T MANE Select	NP_000162.2:p.Pro401=
NM_001146040.2:c.1227A>T	NP_001139512.1:p.Pro409=
NM_001292000.2:c.954A>T	NP_001278929.1:p.Pro318=