Canonical Allele Identifier: CA9047470
Community Standard Title: NM_138393.4(REEP6):c.267G>A (p.Trp89Ter)
Gene: REEP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1495526G>A , CM000681.2:g.1495526G>A GRCh38
NC_000019.9:g.1495525G>A , CM000681.1:g.1495525G>A GRCh37
NC_000019.8:g.1446525G>A NCBI36
NG_055254.1:g.9522G>A

Transcript Alleles

HGVS Amino-acid Change
NM_138393.4:c.267G>A MANE Select NP_612402.1:p.Trp89Ter
ENST00000233596.8:c.267G>A MANE Select ENSP00000233596.2:p.Trp89Ter
NM_001329556.3:c.267G>A MANE Plus Clinical NP_001316485.1:p.Trp89Ter
ENST00000395479.10:c.267G>A MANE Plus Clinical ENSP00000378861.5:p.Trp89Ter
NM_001329556.2:c.267G>A NP_001316485.1:p.Trp89Ter
NM_138393.1:c.267G>A NP_612402.1:p.Trp89Ter
NM_138393.3:c.267G>A NP_612402.1:p.Trp89Ter
ENST00000233596.7:c.267G>A ENSP00000233596.2:p.Trp89Ter
ENST00000395479.8:c.83G>A
ENST00000395484.4:c.51G>A ENSP00000378865.4:p.Trp17Ter
ENST00000591735.2:n.371G>A