Canonical Allele Identifier: CA563958365
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1561543747

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151823029del , CM000667.2:g.151823029del GRCh38
NC_000005.9:g.151202590del , CM000667.1:g.151202590del GRCh37
NC_000005.8:g.151182783del NCBI36
NG_011764.1:g.106809del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1060-65del MANE Select ENSP00000274576.5:n.1060-65del
ENST00000274576.8:c.1060-65del ENSP00000274576.4:n.1060-65del
ENST00000455880.2:c.1060-41del ENSP00000411593.2:n.1060-41del
ENST00000462581.6:c.*818-65del ENSP00000430595.1:n.*818-65del
NM_000171.3:c.1060-65del NP_000162.2:n.1060-65del
NM_001146040.1:c.1060-41del NP_001139512.1:n.1060-41del
NM_001292000.1:c.811-65del NP_001278929.1:n.811-65del
NM_000171.4:c.1060-65del MANE Select NP_000162.2:n.1060-65del
NM_001146040.2:c.1060-41del NP_001139512.1:n.1060-41del
NM_001292000.2:c.811-65del NP_001278929.1:n.811-65del