Canonical Allele Identifier: CA6212736
Gene: TMEM126A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.85654264C>A , CM000673.2:g.85654264C>A GRCh38
NC_000011.9:g.85365308C>A , CM000673.1:g.85365308C>A GRCh37
NC_000011.8:g.85042956C>A NCBI36
NG_017157.1:g.11346C>A
NG_017157.2:g.11346C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304511.7:c.280+8C>A MANE Select ENSP00000306887.2:n.280+8C>A
ENST00000304511.6:c.280+8C>A ENSP00000306887.2:n.280+8C>A
ENST00000525353.5:c.*160+30C>A ENSP00000431993.1:n.*160+30C>A
ENST00000528105.5:c.70+8C>A ENSP00000436590.1:n.70+8C>A
ENST00000531366.5:c.258+30C>A ENSP00000436723.1:n.258+30C>A
ENST00000532180.1:c.70+8C>A ENSP00000434357.1:n.70+8C>A
NM_001244735.1:c.70+8C>A NP_001231664.1:n.70+8C>A
NM_032273.3:c.280+8C>A NP_115649.1:n.280+8C>A
NM_032273.4:c.280+8C>A MANE Select NP_115649.1:n.280+8C>A
NM_001244735.2:c.70+8C>A NP_001231664.1:n.70+8C>A