Canonical Allele Identifier: CA805722679
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1368681533
MyVariant Identifiers: chr5:g.151202565del (hg19) chr5:g.151823004del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151823004del , CM000667.2:g.151823004del GRCh38
NC_000005.9:g.151202565del , CM000667.1:g.151202565del GRCh37
NC_000005.8:g.151182758del NCBI36
NG_011764.1:g.106833del

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1060-41del MANE Select ENSP00000274576.5:n.1060-41del
ENST00000274576.8:c.1060-41del ENSP00000274576.4:n.1060-41del
ENST00000455880.2:c.1060-17del ENSP00000411593.2:n.1060-17del
ENST00000462581.6:c.*818-41del ENSP00000430595.1:n.*818-41del
NM_000171.3:c.1060-41del NP_000162.2:n.1060-41del
NM_001146040.1:c.1060-17del NP_001139512.1:n.1060-17del
NM_001292000.1:c.811-41del NP_001278929.1:n.811-41del
NM_000171.4:c.1060-41del MANE Select NP_000162.2:n.1060-41del
NM_001146040.2:c.1060-17del NP_001139512.1:n.1060-17del
NM_001292000.2:c.811-41del NP_001278929.1:n.811-41del
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