Canonical Allele Identifier: CA2466677470
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154419746G= , CM000685.2:g.154419746G= GRCh38
NC_000023.10:g.153648085G= , CM000685.1:g.153648085G= GRCh37
NC_000023.9:g.153301279G= NCBI36
NG_009634.1:g.13209G=
NG_009634.2:g.13212G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1108G=
ENST00000698317.1:n.1724G=
ENST00000698318.1:n.1507G=
ENST00000698319.1:n.870G=
ENST00000698320.1:n.758G=
ENST00000470127.2:n.771G=
ENST00000475699.6:c.547G= ENSP00000419854.3:p.Gly183=
ENST00000483674.3:n.465G=
ENST00000601016.6:c.583G= MANE Select ENSP00000469981.1:p.Gly195=
ENST00000612012.5:c.541+123G= ENSP00000482070.2:n.541+123G=
ENST00000612460.5:c.493G= ENSP00000481037.1:p.Gly165=
ENST00000614595.2:n.1930G=
ENST00000615658.5:n.887G=
ENST00000616020.5:c.595+123G= ENSP00000483636.2:n.595+123G=
ENST00000617701.5:c.*311G= ENSP00000481645.1:n.*311G=
ENST00000652354.1:c.265+123G= ENSP00000498734.1:n.265+123G=
ENST00000652358.1:c.376G= ENSP00000498464.1:p.Gly126=
ENST00000652390.1:c.502G= ENSP00000498858.1:p.Gly168=
ENST00000652476.1:n.964G=
ENST00000652644.1:c.196G= ENSP00000498496.1:p.Gly66=
ENST00000652682.1:c.640G= ENSP00000498288.1:p.Gly214=
ENST00000652685.1:n.651G=
ENST00000369776.8:c.376+123G= ENSP00000358791.4:n.376+123G=
ENST00000426231.5:c.580G=
ENST00000439735.2:c.490G= ENSP00000398193.1:p.Gly164=
ENST00000470127.1:n.162G=
ENST00000475699.5:c.541+123G= ENSP00000419854.2:n.541+123G=
ENST00000476679.5:n.577G=
ENST00000483780.5:n.348G=
ENST00000494912.5:n.1272G=
ENST00000601016.5:c.583G= ENSP00000469981.1:p.Gly195=
ENST00000612012.4:c.547G= ENSP00000482070.1:p.Gly183=
ENST00000612460.4:c.493G= ENSP00000481037.1:p.Gly165=
ENST00000613002.4:c.451+123G= ENSP00000478154.1:n.451+123G=
ENST00000613634.4:n.813G=
ENST00000615658.4:n.987G=
ENST00000615986.4:c.*311G= ENSP00000480133.1:n.*311G=
ENST00000620808.4:c.*170-286G= ENSP00000479311.1:n.*170-286G=
NM_000116.4:c.583G= NP_000107.1:p.Gly195=
NM_001303465.1:c.595+123G= NP_001290394.1:n.595+123G=
NM_181311.3:c.493G= NP_851828.1:p.Gly165=
NM_181312.3:c.541+123G= NP_851829.1:n.541+123G=
NM_181313.3:c.451+123G= NP_851830.1:n.451+123G=
NR_024048.2:n.925G=
XM_006724836.1:c.637G= XP_006724899.1:p.Gly213=
XM_006724837.1:c.505+123G= XP_006724900.1:n.505+123G=
XM_006724839.1:c.505+123G= XP_006724902.1:n.505+123G=
XM_006724841.2:c.376G= XP_006724904.1:p.Gly126=
XM_006724842.2:c.286G= XP_006724905.1:p.Gly96=
XM_011531189.1:c.425-286G= XP_011529491.1:n.425-286G=
XM_011531190.1:c.376G= XP_011529492.1:p.Gly126=
XM_011531191.1:c.307G= XP_011529493.1:p.Gly103=
XM_011531192.1:c.304G= XP_011529494.1:p.Gly102=
XR_938511.1:n.931G=
XM_006724841.4:c.376G= XP_006724904.1:p.Gly126=
XM_006724842.4:c.286G= XP_006724905.1:p.Gly96=
XM_011531191.2:c.307G= XP_011529493.1:p.Gly103=
XM_017029761.1:c.451+123G= XP_016885250.1:n.451+123G=
XM_017029762.1:c.547G= XP_016885251.1:p.Gly183=
XM_017029763.1:c.371-286G= XP_016885252.1:n.371-286G=
XM_017029764.1:c.304G= XP_016885253.1:p.Gly102=
XM_017029765.2:c.244+123G= XP_016885254.1:n.244+123G=
XM_024452431.1:c.425-286G= XP_024308199.1:n.425-286G=
NM_000116.5:c.583G= MANE Select NP_000107.1:p.Gly195=
NM_001303465.2:c.595+123G= NP_001290394.1:n.595+123G=
NM_181311.4:c.493G= NP_851828.1:p.Gly165=
NM_181312.4:c.541+123G= NP_851829.1:n.541+123G=
NM_181313.4:c.451+123G= NP_851830.1:n.451+123G=
NR_024048.3:n.904G=