Canonical Allele Identifier: CA415180776
Gene: TAFAZZIN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154413251T>A , CM000685.2:g.154413251T>A GRCh38
NC_000023.10:g.153641588T>A , CM000685.1:g.153641588T>A GRCh37
NC_000023.9:g.153294782T>A NCBI36
NG_009634.1:g.6712T>A
NG_012884.2:g.3838A>T
NG_009634.2:g.6717T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698234.1:n.711T>A
ENST00000698235.1:n.270T>A
ENST00000698317.1:n.1237T>A
ENST00000698318.1:n.1098T>A
ENST00000470127.2:n.332T>A
ENST00000475699.6:c.337T>A ENSP00000419854.3:p.Trp113Arg
ENST00000476800.2:n.1240T>A
ENST00000483674.3:n.174T>A
ENST00000601016.6:c.283T>A MANE Select ENSP00000469981.1:p.Trp95Arg
ENST00000612012.5:c.283T>A ENSP00000482070.2:p.Trp95Arg
ENST00000612460.5:c.283T>A ENSP00000481037.1:p.Trp95Arg
ENST00000614595.2:n.1633T>A
ENST00000615658.5:n.596T>A
ENST00000616020.5:c.337T>A ENSP00000483636.2:p.Trp113Arg
ENST00000617701.5:c.283T>A ENSP00000481645.1:p.Trp95Arg
ENST00000621647.2:n.336T>A
ENST00000652354.1:c.7T>A ENSP00000498734.1:p.Trp3Arg
ENST00000652358.1:c.-12T>A ENSP00000498464.1:n.-12T>A
ENST00000652390.1:c.202T>A ENSP00000498858.1:p.Trp68Arg
ENST00000652476.1:n.444T>A
ENST00000652682.1:c.283T>A ENSP00000498288.1:p.Trp95Arg
ENST00000652685.1:n.335T>A
ENST00000369776.8:c.208T>A ENSP00000358791.4:p.Trp70Arg
ENST00000426231.5:c.99T>A
ENST00000439735.2:c.283T>A ENSP00000398193.1:p.Trp95Arg
ENST00000475699.5:c.283T>A ENSP00000419854.2:p.Trp95Arg
ENST00000476679.5:n.196T>A
ENST00000476800.1:n.161T>A
ENST00000479875.1:n.312T>A
ENST00000483780.5:n.57T>A
ENST00000601016.5:c.283T>A ENSP00000469981.1:p.Trp95Arg
ENST00000612012.4:c.337T>A ENSP00000482070.1:p.Trp113Arg
ENST00000612460.4:c.283T>A ENSP00000481037.1:p.Trp95Arg
ENST00000613002.4:c.283T>A ENSP00000478154.1:p.Trp95Arg
ENST00000613634.4:n.603T>A
ENST00000615658.4:n.609T>A
ENST00000615986.4:c.283T>A ENSP00000480133.1:p.Trp95Arg
ENST00000616020.4:c.337T>A ENSP00000483636.1:p.Trp113Arg
ENST00000617701.4:c.283T>A ENSP00000481645.1:p.Trp95Arg
ENST00000620808.4:c.283T>A ENSP00000479311.1:p.Trp95Arg
ENST00000621647.1:n.568T>A
NM_000116.4:c.283T>A NP_000107.1:p.Trp95Arg
NM_001303465.1:c.337T>A NP_001290394.1:p.Trp113Arg
NM_181311.3:c.283T>A NP_851828.1:p.Trp95Arg
NM_181312.3:c.283T>A NP_851829.1:p.Trp95Arg
NM_181313.3:c.283T>A NP_851830.1:p.Trp95Arg
NR_024048.2:n.609T>A
XM_006724836.1:c.337T>A XP_006724899.1:p.Trp113Arg
XM_006724837.1:c.337T>A XP_006724900.1:p.Trp113Arg
XM_006724839.1:c.337T>A XP_006724902.1:p.Trp113Arg
XM_006724841.2:c.-12T>A XP_006724904.1:n.-12T>A
XM_006724842.2:c.-12T>A XP_006724905.1:n.-12T>A
XM_011531189.1:c.337T>A XP_011529491.1:p.Trp113Arg
XM_011531190.1:c.-12T>A XP_011529492.1:n.-12T>A
XM_011531191.1:c.7T>A XP_011529493.1:p.Trp3Arg
XM_011531192.1:c.-115T>A XP_011529494.1:n.-115T>A
XR_938511.1:n.640T>A
XM_006724841.4:c.-12T>A XP_006724904.1:n.-12T>A
XM_006724842.4:c.-12T>A XP_006724905.1:n.-12T>A
XM_011531191.2:c.7T>A XP_011529493.1:p.Trp3Arg
XM_017029761.1:c.283T>A XP_016885250.1:p.Trp95Arg
XM_017029762.1:c.337T>A XP_016885251.1:p.Trp113Arg
XM_017029763.1:c.283T>A XP_016885252.1:p.Trp95Arg
XM_017029764.1:c.-115T>A XP_016885253.1:n.-115T>A
XM_017029765.2:c.-12T>A XP_016885254.1:n.-12T>A
XM_024452431.1:c.337T>A XP_024308199.1:p.Trp113Arg
NM_000116.5:c.283T>A MANE Select NP_000107.1:p.Trp95Arg
NM_001303465.2:c.337T>A NP_001290394.1:p.Trp113Arg
NM_181311.4:c.283T>A NP_851828.1:p.Trp95Arg
NM_181312.4:c.283T>A NP_851829.1:p.Trp95Arg
NM_181313.4:c.283T>A NP_851830.1:p.Trp95Arg
NR_024048.3:n.588T>A