Canonical Allele Identifier: CA447224659

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151231059G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151851498G>A , CM000667.2:g.151851498G>A	GRCh38
NC_000005.9:g.151231059G>A , CM000667.1:g.151231059G>A	GRCh37
NC_000005.8:g.151211252G>A	NCBI36
NG_011764.1:g.78339C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.804C>T MANE Select	ENSP00000274576.5:p.Ile268=
ENST00000274576.8:c.804C>T	ENSP00000274576.4:p.Ile268=
ENST00000455880.2:c.804C>T	ENSP00000411593.2:p.Ile268=
ENST00000462581.6:c.*562C>T	ENSP00000430595.1:n.*562C>T
ENST00000471351.2:n.1087C>T
NM_000171.3:c.804C>T	NP_000162.2:p.Ile268=
NM_001146040.1:c.804C>T	NP_001139512.1:p.Ile268=
NM_001292000.1:c.555C>T	NP_001278929.1:p.Ile185=
XM_005268412.2:c.804C>T	XP_005268469.1:p.Ile268=
NM_000171.4:c.804C>T MANE Select	NP_000162.2:p.Ile268=
NM_001146040.2:c.804C>T	NP_001139512.1:p.Ile268=
NM_001292000.2:c.555C>T	NP_001278929.1:p.Ile185=