Canonical Allele Identifier: CA2676109020
Gene: GLRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151829105C>T , CM000667.2:g.151829105C>T GRCh38
NC_000005.9:g.151208666C>T , CM000667.1:g.151208666C>T GRCh37
NC_000005.8:g.151188859C>T NCBI36
NG_011764.1:g.100732G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000274576.9:c.913-38G>A MANE Select ENSP00000274576.5:n.913-38G>A
ENST00000274576.8:c.913-38G>A ENSP00000274576.4:n.913-38G>A
ENST00000455880.2:c.913-38G>A ENSP00000411593.2:n.913-38G>A
ENST00000462581.6:c.*671-38G>A ENSP00000430595.1:n.*671-38G>A
NM_000171.3:c.913-38G>A NP_000162.2:n.913-38G>A
NM_001146040.1:c.913-38G>A NP_001139512.1:n.913-38G>A
NM_001292000.1:c.664-38G>A NP_001278929.1:n.664-38G>A
NM_000171.4:c.913-38G>A MANE Select NP_000162.2:n.913-38G>A
NM_001146040.2:c.913-38G>A NP_001139512.1:n.913-38G>A
NM_001292000.2:c.664-38G>A NP_001278929.1:n.664-38G>A