Canonical Allele Identifier: CA2466677627
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420240G= , CM000685.2:g.154420240G= GRCh38
NC_000023.10:g.153648579G= , CM000685.1:g.153648579G= GRCh37
NC_000023.9:g.153301773G= NCBI36
NG_009634.1:g.13703G=
NG_009634.2:g.13706G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1485G=
ENST00000698317.1:n.2101G=
ENST00000698318.1:n.1884G=
ENST00000698319.1:n.1247G=
ENST00000698320.1:n.1135G=
ENST00000470127.2:n.1148G=
ENST00000475699.6:c.639G= ENSP00000419854.3:p.Pro213=
ENST00000483674.3:n.557G=
ENST00000601016.6:c.675G= MANE Select ENSP00000469981.1:p.Pro225=
ENST00000612012.5:c.633G= ENSP00000482070.2:p.Pro211=
ENST00000612460.5:c.585G= ENSP00000481037.1:p.Pro195=
ENST00000614595.2:n.2022G=
ENST00000615658.5:n.1264G=
ENST00000616020.5:c.687G= ENSP00000483636.2:p.Pro229=
ENST00000617701.5:c.*688G= ENSP00000481645.1:n.*688G=
ENST00000652354.1:c.357G= ENSP00000498734.1:p.Pro119=
ENST00000652358.1:c.468G= ENSP00000498464.1:p.Pro156=
ENST00000652390.1:c.594G= ENSP00000498858.1:p.Pro198=
ENST00000652476.1:n.1341G=
ENST00000652644.1:c.288G= ENSP00000498496.1:p.Pro96=
ENST00000652682.1:c.732G= ENSP00000498288.1:p.Pro244=
ENST00000652685.1:n.1028G=
ENST00000369776.8:c.585G= ENSP00000358791.4:p.Pro195=
ENST00000426231.5:c.672G=
ENST00000475699.5:c.633G= ENSP00000419854.2:p.Pro211=
ENST00000494912.5:n.1364G=
ENST00000498029.1:n.133G=
ENST00000601016.5:c.675G= ENSP00000469981.1:p.Pro225=
ENST00000612460.4:c.585G= ENSP00000481037.1:p.Pro195=
ENST00000613002.4:c.543G= ENSP00000478154.1:p.Pro181=
ENST00000615986.4:c.*403G= ENSP00000480133.1:n.*403G=
NM_000116.4:c.675G= NP_000107.1:p.Pro225=
NM_001303465.1:c.687G= NP_001290394.1:p.Pro229=
NM_181311.3:c.585G= NP_851828.1:p.Pro195=
NM_181312.3:c.633G= NP_851829.1:p.Pro211=
NM_181313.3:c.543G= NP_851830.1:p.Pro181=
NR_024048.2:n.1017G=
XM_006724836.1:c.729G= XP_006724899.1:p.Pro243=
XM_006724837.1:c.714G= XP_006724900.1:p.Pro238=
XM_006724839.1:c.597G= XP_006724902.1:p.Pro199=
XM_006724841.2:c.468G= XP_006724904.1:p.Pro156=
XM_006724842.2:c.378G= XP_006724905.1:p.Pro126=
XM_011531189.1:c.516G= XP_011529491.1:p.Pro172=
XM_011531190.1:c.468G= XP_011529492.1:p.Pro156=
XM_011531191.1:c.399G= XP_011529493.1:p.Pro133=
XM_011531192.1:c.396G= XP_011529494.1:p.Pro132=
XR_938511.1:n.1023G=
XM_006724841.4:c.468G= XP_006724904.1:p.Pro156=
XM_006724842.4:c.378G= XP_006724905.1:p.Pro126=
XM_011531191.2:c.399G= XP_011529493.1:p.Pro133=
XM_017029761.1:c.660G= XP_016885250.1:p.Pro220=
XM_017029762.1:c.639G= XP_016885251.1:p.Pro213=
XM_017029763.1:c.462G= XP_016885252.1:p.Pro154=
XM_017029764.1:c.396G= XP_016885253.1:p.Pro132=
XM_017029765.2:c.336G= XP_016885254.1:p.Pro112=
XM_024452431.1:c.633G= XP_024308199.1:p.Pro211=
NM_000116.5:c.675G= MANE Select NP_000107.1:p.Pro225=
NM_001303465.2:c.687G= NP_001290394.1:p.Pro229=
NM_181311.4:c.585G= NP_851828.1:p.Pro195=
NM_181312.4:c.633G= NP_851829.1:p.Pro211=
NM_181313.4:c.543G= NP_851830.1:p.Pro181=
NR_024048.3:n.996G=