Canonical Allele Identifier: CA2466677468
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154419742G= , CM000685.2:g.154419742G= GRCh38
NC_000023.10:g.153648081G= , CM000685.1:g.153648081G= GRCh37
NC_000023.9:g.153301275G= NCBI36
NG_009634.1:g.13205G=
NG_009634.2:g.13208G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1104G=
ENST00000698317.1:n.1720G=
ENST00000698318.1:n.1503G=
ENST00000698319.1:n.866G=
ENST00000698320.1:n.754G=
ENST00000470127.2:n.767G=
ENST00000475699.6:c.543G= ENSP00000419854.3:p.Lys181=
ENST00000483674.3:n.461G=
ENST00000601016.6:c.579G= MANE Select ENSP00000469981.1:p.Lys193=
ENST00000612012.5:c.541+119G= ENSP00000482070.2:n.541+119G=
ENST00000612460.5:c.489G= ENSP00000481037.1:p.Lys163=
ENST00000614595.2:n.1926G=
ENST00000615658.5:n.883G=
ENST00000616020.5:c.595+119G= ENSP00000483636.2:n.595+119G=
ENST00000617701.5:c.*307G= ENSP00000481645.1:n.*307G=
ENST00000652354.1:c.265+119G= ENSP00000498734.1:n.265+119G=
ENST00000652358.1:c.372G= ENSP00000498464.1:p.Lys124=
ENST00000652390.1:c.498G= ENSP00000498858.1:p.Lys166=
ENST00000652476.1:n.960G=
ENST00000652644.1:c.192G= ENSP00000498496.1:p.Lys64=
ENST00000652682.1:c.636G= ENSP00000498288.1:p.Lys212=
ENST00000652685.1:n.647G=
ENST00000369776.8:c.376+119G= ENSP00000358791.4:n.376+119G=
ENST00000426231.5:c.576G=
ENST00000439735.2:c.486G= ENSP00000398193.1:p.Lys162=
ENST00000470127.1:n.158G=
ENST00000475699.5:c.541+119G= ENSP00000419854.2:n.541+119G=
ENST00000476679.5:n.573G=
ENST00000483780.5:n.344G=
ENST00000494912.5:n.1268G=
ENST00000601016.5:c.579G= ENSP00000469981.1:p.Lys193=
ENST00000612012.4:c.543G= ENSP00000482070.1:p.Lys181=
ENST00000612460.4:c.489G= ENSP00000481037.1:p.Lys163=
ENST00000613002.4:c.451+119G= ENSP00000478154.1:n.451+119G=
ENST00000613634.4:n.809G=
ENST00000615658.4:n.983G=
ENST00000615986.4:c.*307G= ENSP00000480133.1:n.*307G=
ENST00000620808.4:c.*170-290G= ENSP00000479311.1:n.*170-290G=
NM_000116.4:c.579G= NP_000107.1:p.Lys193=
NM_001303465.1:c.595+119G= NP_001290394.1:n.595+119G=
NM_181311.3:c.489G= NP_851828.1:p.Lys163=
NM_181312.3:c.541+119G= NP_851829.1:n.541+119G=
NM_181313.3:c.451+119G= NP_851830.1:n.451+119G=
NR_024048.2:n.921G=
XM_006724836.1:c.633G= XP_006724899.1:p.Lys211=
XM_006724837.1:c.505+119G= XP_006724900.1:n.505+119G=
XM_006724839.1:c.505+119G= XP_006724902.1:n.505+119G=
XM_006724841.2:c.372G= XP_006724904.1:p.Lys124=
XM_006724842.2:c.282G= XP_006724905.1:p.Lys94=
XM_011531189.1:c.425-290G= XP_011529491.1:n.425-290G=
XM_011531190.1:c.372G= XP_011529492.1:p.Lys124=
XM_011531191.1:c.303G= XP_011529493.1:p.Lys101=
XM_011531192.1:c.300G= XP_011529494.1:p.Lys100=
XR_938511.1:n.927G=
XM_006724841.4:c.372G= XP_006724904.1:p.Lys124=
XM_006724842.4:c.282G= XP_006724905.1:p.Lys94=
XM_011531191.2:c.303G= XP_011529493.1:p.Lys101=
XM_017029761.1:c.451+119G= XP_016885250.1:n.451+119G=
XM_017029762.1:c.543G= XP_016885251.1:p.Lys181=
XM_017029763.1:c.371-290G= XP_016885252.1:n.371-290G=
XM_017029764.1:c.300G= XP_016885253.1:p.Lys100=
XM_017029765.2:c.244+119G= XP_016885254.1:n.244+119G=
XM_024452431.1:c.425-290G= XP_024308199.1:n.425-290G=
NM_000116.5:c.579G= MANE Select NP_000107.1:p.Lys193=
NM_001303465.2:c.595+119G= NP_001290394.1:n.595+119G=
NM_181311.4:c.489G= NP_851828.1:p.Lys163=
NM_181312.4:c.541+119G= NP_851829.1:n.541+119G=
NM_181313.4:c.451+119G= NP_851830.1:n.451+119G=
NR_024048.3:n.900G=