Canonical Allele Identifier: CA364153214
Community Standard Title: NM_000287.4(PEX6):c.1908T>A (p.Tyr636Ter)
Gene: PEX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.42966835A>T , CM000668.2:g.42966835A>T GRCh38
NC_000006.11:g.42934573A>T , CM000668.1:g.42934573A>T GRCh37
NC_000006.10:g.43042551A>T NCBI36
NG_008370.1:g.17409T>A

Transcript Alleles

HGVS Amino-acid Change
NM_000287.4:c.1908T>A MANE Select NP_000278.3:p.Tyr636Ter
ENST00000304611.13:c.1908T>A MANE Select ENSP00000303511.8:p.Tyr636Ter
NM_000287.3:c.1908T>A NP_000278.3:p.Tyr636Ter
NM_001316313.1:c.1644T>A NP_001303242.1:p.Tyr548Ter
NM_001316313.2:c.1644T>A NP_001303242.1:p.Tyr548Ter
NR_133009.1:n.2001T>A
NR_133009.2:n.1939T>A
ENST00000244546.4:c.1908T>A ENSP00000244546.4:p.Tyr636Ter
ENST00000304611.12:c.1908T>A ENSP00000303511.8:p.Tyr636Ter
XM_011514661.1:c.1824T>A XP_011512963.1:p.Tyr608Ter
XM_011514661.2:c.1824T>A XP_011512963.1:p.Tyr608Ter
XR_001743466.2:n.2870T>A
XR_926246.1:n.1889T>A