Canonical Allele Identifier: CA2466677568
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420037G= , CM000685.2:g.154420037G= GRCh38
NC_000023.10:g.153648376G= , CM000685.1:g.153648376G= GRCh37
NC_000023.9:g.153301570G= NCBI36
NG_009634.1:g.13500G=
NG_009634.2:g.13503G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1399G=
ENST00000698317.1:n.2015G=
ENST00000698318.1:n.1798G=
ENST00000698319.1:n.1161G=
ENST00000698320.1:n.1049G=
ENST00000470127.2:n.1062G=
ENST00000475699.6:c.553G= ENSP00000419854.3:p.Gly185=
ENST00000483674.3:n.471G=
ENST00000601016.6:c.589G= MANE Select ENSP00000469981.1:p.Gly197=
ENST00000612012.5:c.547G= ENSP00000482070.2:p.Gly183=
ENST00000612460.5:c.499G= ENSP00000481037.1:p.Gly167=
ENST00000614595.2:n.1936G=
ENST00000615658.5:n.1178G=
ENST00000616020.5:c.601G= ENSP00000483636.2:p.Gly201=
ENST00000617701.5:c.*602G= ENSP00000481645.1:n.*602G=
ENST00000652354.1:c.271G= ENSP00000498734.1:p.Gly91=
ENST00000652358.1:c.382G= ENSP00000498464.1:p.Gly128=
ENST00000652390.1:c.508G= ENSP00000498858.1:p.Gly170=
ENST00000652476.1:n.1255G=
ENST00000652644.1:c.202G= ENSP00000498496.1:p.Gly68=
ENST00000652682.1:c.646G= ENSP00000498288.1:p.Gly216=
ENST00000652685.1:n.942G=
ENST00000369776.8:c.382G= ENSP00000358791.4:p.Gly128=
ENST00000426231.5:c.586G=
ENST00000439735.2:c.496G= ENSP00000398193.1:p.Gly166=
ENST00000470127.1:n.168G=
ENST00000475699.5:c.547G= ENSP00000419854.2:p.Gly183=
ENST00000494912.5:n.1278G=
ENST00000498029.1:n.47G=
ENST00000601016.5:c.589G= ENSP00000469981.1:p.Gly197=
ENST00000612012.4:c.553G= ENSP00000482070.1:p.Gly185=
ENST00000612460.4:c.499G= ENSP00000481037.1:p.Gly167=
ENST00000613002.4:c.457G= ENSP00000478154.1:p.Gly153=
ENST00000613634.4:n.1104G=
ENST00000615658.4:n.1278G=
ENST00000615986.4:c.*317G= ENSP00000480133.1:n.*317G=
ENST00000620808.4:c.*175G= ENSP00000479311.1:n.*175G=
NM_000116.4:c.589G= NP_000107.1:p.Gly197=
NM_001303465.1:c.601G= NP_001290394.1:p.Gly201=
NM_181311.3:c.499G= NP_851828.1:p.Gly167=
NM_181312.3:c.547G= NP_851829.1:p.Gly183=
NM_181313.3:c.457G= NP_851830.1:p.Gly153=
NR_024048.2:n.931G=
XM_006724836.1:c.643G= XP_006724899.1:p.Gly215=
XM_006724837.1:c.511G= XP_006724900.1:p.Gly171=
XM_006724839.1:c.511G= XP_006724902.1:p.Gly171=
XM_006724841.2:c.382G= XP_006724904.1:p.Gly128=
XM_006724842.2:c.292G= XP_006724905.1:p.Gly98=
XM_011531189.1:c.430G= XP_011529491.1:p.Gly144=
XM_011531190.1:c.382G= XP_011529492.1:p.Gly128=
XM_011531191.1:c.313G= XP_011529493.1:p.Gly105=
XM_011531192.1:c.310G= XP_011529494.1:p.Gly104=
XR_938511.1:n.937G=
XM_006724841.4:c.382G= XP_006724904.1:p.Gly128=
XM_006724842.4:c.292G= XP_006724905.1:p.Gly98=
XM_011531191.2:c.313G= XP_011529493.1:p.Gly105=
XM_017029761.1:c.457G= XP_016885250.1:p.Gly153=
XM_017029762.1:c.553G= XP_016885251.1:p.Gly185=
XM_017029763.1:c.376G= XP_016885252.1:p.Gly126=
XM_017029764.1:c.310G= XP_016885253.1:p.Gly104=
XM_017029765.2:c.250G= XP_016885254.1:p.Gly84=
XM_024452431.1:c.430G= XP_024308199.1:p.Gly144=
NM_000116.5:c.589G= MANE Select NP_000107.1:p.Gly197=
NM_001303465.2:c.601G= NP_001290394.1:p.Gly201=
NM_181311.4:c.499G= NP_851828.1:p.Gly167=
NM_181312.4:c.547G= NP_851829.1:p.Gly183=
NM_181313.4:c.457G= NP_851830.1:p.Gly153=
NR_024048.3:n.910G=