Canonical Allele Identifier: CA2466677578
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420069C= , CM000685.2:g.154420069C= GRCh38
NC_000023.10:g.153648408C= , CM000685.1:g.153648408C= GRCh37
NC_000023.9:g.153301602C= NCBI36
NG_009634.1:g.13532C=
NG_009634.2:g.13535C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1431C=
ENST00000698317.1:n.2047C=
ENST00000698318.1:n.1830C=
ENST00000698319.1:n.1193C=
ENST00000698320.1:n.1081C=
ENST00000470127.2:n.1094C=
ENST00000475699.6:c.585C= ENSP00000419854.3:p.Pro195=
ENST00000483674.3:n.503C=
ENST00000601016.6:c.621C= MANE Select ENSP00000469981.1:p.Pro207=
ENST00000612012.5:c.579C= ENSP00000482070.2:p.Pro193=
ENST00000612460.5:c.531C= ENSP00000481037.1:p.Pro177=
ENST00000614595.2:n.1968C=
ENST00000615658.5:n.1210C=
ENST00000616020.5:c.633C= ENSP00000483636.2:p.Pro211=
ENST00000617701.5:c.*634C= ENSP00000481645.1:n.*634C=
ENST00000652354.1:c.303C= ENSP00000498734.1:p.Pro101=
ENST00000652358.1:c.414C= ENSP00000498464.1:p.Pro138=
ENST00000652390.1:c.540C= ENSP00000498858.1:p.Pro180=
ENST00000652476.1:n.1287C=
ENST00000652644.1:c.234C= ENSP00000498496.1:p.Pro78=
ENST00000652682.1:c.678C= ENSP00000498288.1:p.Pro226=
ENST00000652685.1:n.974C=
ENST00000369776.8:c.414C= ENSP00000358791.4:p.Pro138=
ENST00000426231.5:c.618C=
ENST00000439735.2:c.528C= ENSP00000398193.1:p.Pro176=
ENST00000470127.1:n.200C=
ENST00000475699.5:c.579C= ENSP00000419854.2:p.Pro193=
ENST00000494912.5:n.1310C=
ENST00000498029.1:n.79C=
ENST00000601016.5:c.621C= ENSP00000469981.1:p.Pro207=
ENST00000612012.4:c.585C= ENSP00000482070.1:p.Pro195=
ENST00000612460.4:c.531C= ENSP00000481037.1:p.Pro177=
ENST00000613002.4:c.489C= ENSP00000478154.1:p.Pro163=
ENST00000615658.4:n.1310C=
ENST00000615986.4:c.*349C= ENSP00000480133.1:n.*349C=
ENST00000620808.4:c.*207C= ENSP00000479311.1:n.*207C=
NM_000116.4:c.621C= NP_000107.1:p.Pro207=
NM_001303465.1:c.633C= NP_001290394.1:p.Pro211=
NM_181311.3:c.531C= NP_851828.1:p.Pro177=
NM_181312.3:c.579C= NP_851829.1:p.Pro193=
NM_181313.3:c.489C= NP_851830.1:p.Pro163=
NR_024048.2:n.963C=
XM_006724836.1:c.675C= XP_006724899.1:p.Pro225=
XM_006724837.1:c.543C= XP_006724900.1:p.Pro181=
XM_006724839.1:c.543C= XP_006724902.1:p.Pro181=
XM_006724841.2:c.414C= XP_006724904.1:p.Pro138=
XM_006724842.2:c.324C= XP_006724905.1:p.Pro108=
XM_011531189.1:c.462C= XP_011529491.1:p.Pro154=
XM_011531190.1:c.414C= XP_011529492.1:p.Pro138=
XM_011531191.1:c.345C= XP_011529493.1:p.Pro115=
XM_011531192.1:c.342C= XP_011529494.1:p.Pro114=
XR_938511.1:n.969C=
XM_006724841.4:c.414C= XP_006724904.1:p.Pro138=
XM_006724842.4:c.324C= XP_006724905.1:p.Pro108=
XM_011531191.2:c.345C= XP_011529493.1:p.Pro115=
XM_017029761.1:c.489C= XP_016885250.1:p.Pro163=
XM_017029762.1:c.585C= XP_016885251.1:p.Pro195=
XM_017029763.1:c.408C= XP_016885252.1:p.Pro136=
XM_017029764.1:c.342C= XP_016885253.1:p.Pro114=
XM_017029765.2:c.282C= XP_016885254.1:p.Pro94=
XM_024452431.1:c.462C= XP_024308199.1:p.Pro154=
NM_000116.5:c.621C= MANE Select NP_000107.1:p.Pro207=
NM_001303465.2:c.633C= NP_001290394.1:p.Pro211=
NM_181311.4:c.531C= NP_851828.1:p.Pro177=
NM_181312.4:c.579C= NP_851829.1:p.Pro193=
NM_181313.4:c.489C= NP_851830.1:p.Pro163=
NR_024048.3:n.942C=