Canonical Allele Identifier: CA2710198182
Gene: GLRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2113289596

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151828885A>T , CM000667.2:g.151828885A>T GRCh38
NC_000005.9:g.151208446A>T , CM000667.1:g.151208446A>T GRCh37
NC_000005.8:g.151188639A>T NCBI36
NG_011764.1:g.100952T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.1059+36T>A MANE Select ENSP00000274576.5:n.1059+36T>A
ENST00000274576.8:c.1059+36T>A ENSP00000274576.4:n.1059+36T>A
ENST00000455880.2:c.1059+36T>A ENSP00000411593.2:n.1059+36T>A
ENST00000462581.6:c.*817+36T>A ENSP00000430595.1:n.*817+36T>A
NM_000171.3:c.1059+36T>A NP_000162.2:n.1059+36T>A
NM_001146040.1:c.1059+36T>A NP_001139512.1:n.1059+36T>A
NM_001292000.1:c.810+36T>A NP_001278929.1:n.810+36T>A
NM_000171.4:c.1059+36T>A MANE Select NP_000162.2:n.1059+36T>A
NM_001146040.2:c.1059+36T>A NP_001139512.1:n.1059+36T>A
NM_001292000.2:c.810+36T>A NP_001278929.1:n.810+36T>A