Canonical Allele Identifier: CA2466677805
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420731C= , CM000685.2:g.154420731C= GRCh38
NC_000023.10:g.153649070C= , CM000685.1:g.153649070C= GRCh37
NC_000023.9:g.153302264C= NCBI36
NG_009634.1:g.14194C=
NG_009634.2:g.14197C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1583C=
ENST00000698317.1:n.2199C=
ENST00000698318.1:n.1982C=
ENST00000698319.1:n.1345C=
ENST00000698320.1:n.1233C=
ENST00000470127.2:n.1246C=
ENST00000475699.6:c.737C= ENSP00000419854.3:p.Ser246=
ENST00000483674.3:n.655C=
ENST00000601016.6:c.773C= MANE Select ENSP00000469981.1:p.Ser258=
ENST00000612012.5:c.731C= ENSP00000482070.2:p.Ser244=
ENST00000612460.5:c.683C= ENSP00000481037.1:p.Ser228=
ENST00000614595.2:n.2120C=
ENST00000615658.5:n.1362C=
ENST00000616020.5:c.785C= ENSP00000483636.2:p.Ser262=
ENST00000617701.5:c.*786C= ENSP00000481645.1:n.*786C=
ENST00000651139.1:c.-11C= ENSP00000498957.1:n.-11C=
ENST00000652354.1:c.455C= ENSP00000498734.1:p.Ser152=
ENST00000652358.1:c.566C= ENSP00000498464.1:p.Ser189=
ENST00000652390.1:c.692C= ENSP00000498858.1:p.Ser231=
ENST00000652476.1:n.1439C=
ENST00000652644.1:c.386C= ENSP00000498496.1:p.Ser129=
ENST00000652682.1:c.830C= ENSP00000498288.1:p.Ser277=
ENST00000652685.1:n.1126C=
ENST00000369776.8:c.683C= ENSP00000358791.4:p.Ser228=
ENST00000426231.5:c.770C=
ENST00000475699.5:c.731C= ENSP00000419854.2:p.Ser244=
ENST00000494912.5:n.1462C=
ENST00000498029.1:n.231C=
ENST00000601016.5:c.773C= ENSP00000469981.1:p.Ser258=
ENST00000612460.4:c.683C= ENSP00000481037.1:p.Ser228=
ENST00000613002.4:c.641C= ENSP00000478154.1:p.Ser214=
ENST00000615986.4:c.*501C= ENSP00000480133.1:n.*501C=
NM_000116.4:c.773C= NP_000107.1:p.Ser258=
NM_001303465.1:c.785C= NP_001290394.1:p.Ser262=
NM_181311.3:c.683C= NP_851828.1:p.Ser228=
NM_181312.3:c.731C= NP_851829.1:p.Ser244=
NM_181313.3:c.641C= NP_851830.1:p.Ser214=
NR_024048.2:n.1115C=
XM_006724836.1:c.827C= XP_006724899.1:p.Ser276=
XM_006724837.1:c.812C= XP_006724900.1:p.Ser271=
XM_006724839.1:c.695C= XP_006724902.1:p.Ser232=
XM_006724841.2:c.566C= XP_006724904.1:p.Ser189=
XM_006724842.2:c.476C= XP_006724905.1:p.Ser159=
XM_011531189.1:c.614C= XP_011529491.1:p.Ser205=
XM_011531190.1:c.566C= XP_011529492.1:p.Ser189=
XM_011531191.1:c.497C= XP_011529493.1:p.Ser166=
XM_011531192.1:c.494C= XP_011529494.1:p.Ser165=
XR_938511.1:n.1121C=
XM_006724841.4:c.566C= XP_006724904.1:p.Ser189=
XM_006724842.4:c.476C= XP_006724905.1:p.Ser159=
XM_011531191.2:c.497C= XP_011529493.1:p.Ser166=
XM_017029761.1:c.758C= XP_016885250.1:p.Ser253=
XM_017029762.1:c.737C= XP_016885251.1:p.Ser246=
XM_017029763.1:c.560C= XP_016885252.1:p.Ser187=
XM_017029764.1:c.494C= XP_016885253.1:p.Ser165=
XM_017029765.2:c.434C= XP_016885254.1:p.Ser145=
XM_024452431.1:c.731C= XP_024308199.1:p.Ser244=
NM_000116.5:c.773C= MANE Select NP_000107.1:p.Ser258=
NM_001303465.2:c.785C= NP_001290394.1:p.Ser262=
NM_181311.4:c.683C= NP_851828.1:p.Ser228=
NM_181312.4:c.731C= NP_851829.1:p.Ser244=
NM_181313.4:c.641C= NP_851830.1:p.Ser214=
NR_024048.3:n.1094C=