Canonical Allele Identifier: CA447226569

Gene: GLRA1

Linked Data

• MyVariant Identifiers: chr5:g.151202348G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151822787G>C , CM000667.2:g.151822787G>C	GRCh38
NC_000005.9:g.151202348G>C , CM000667.1:g.151202348G>C	GRCh37
NC_000005.8:g.151182541G>C	NCBI36
NG_011764.1:g.107050C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274576.9:c.1236C>G MANE Select	ENSP00000274576.5:p.Ala412=
ENST00000274576.8:c.1236C>G	ENSP00000274576.4:p.Ala412=
ENST00000455880.2:c.1260C>G	ENSP00000411593.2:p.Ala420=
ENST00000462581.6:c.*994C>G	ENSP00000430595.1:n.*994C>G
NM_000171.3:c.1236C>G	NP_000162.2:p.Ala412=
NM_001146040.1:c.1260C>G	NP_001139512.1:p.Ala420=
NM_001292000.1:c.987C>G	NP_001278929.1:p.Ala329=
NM_000171.4:c.1236C>G MANE Select	NP_000162.2:p.Ala412=
NM_001146040.2:c.1260C>G	NP_001139512.1:p.Ala420=
NM_001292000.2:c.987C>G	NP_001278929.1:p.Ala329=