Canonical Allele Identifier: CA2466677674
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420371T= , CM000685.2:g.154420371T= GRCh38
NC_000023.10:g.153648710T= , CM000685.1:g.153648710T= GRCh37
NC_000023.9:g.153301904T= NCBI36
NG_009634.1:g.13834T=
NG_009634.2:g.13837T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1509+107T=
ENST00000698317.1:n.2125+107T=
ENST00000698318.1:n.1908+107T=
ENST00000698319.1:n.1271+107T=
ENST00000698320.1:n.1159+107T=
ENST00000470127.2:n.1172+107T=
ENST00000475699.6:c.663+107T= ENSP00000419854.3:n.663+107T=
ENST00000483674.3:n.581+107T=
ENST00000601016.6:c.699+107T= MANE Select ENSP00000469981.1:n.699+107T=
ENST00000612012.5:c.657+107T= ENSP00000482070.2:n.657+107T=
ENST00000612460.5:c.609+107T= ENSP00000481037.1:n.609+107T=
ENST00000614595.2:n.2046+107T=
ENST00000615658.5:n.1288+107T=
ENST00000616020.5:c.711+107T= ENSP00000483636.2:n.711+107T=
ENST00000617701.5:c.*712+107T= ENSP00000481645.1:n.*712+107T=
ENST00000651139.1:c.-173T= ENSP00000498957.1:n.-173T=
ENST00000652354.1:c.381+107T= ENSP00000498734.1:n.381+107T=
ENST00000652358.1:c.492+107T= ENSP00000498464.1:n.492+107T=
ENST00000652390.1:c.618+107T= ENSP00000498858.1:n.618+107T=
ENST00000652476.1:n.1365+107T=
ENST00000652644.1:c.312+107T= ENSP00000498496.1:n.312+107T=
ENST00000652682.1:c.756+107T= ENSP00000498288.1:n.756+107T=
ENST00000652685.1:n.1052+107T=
ENST00000369776.8:c.609+107T= ENSP00000358791.4:n.609+107T=
ENST00000426231.5:c.696+107T=
ENST00000475699.5:c.657+107T= ENSP00000419854.2:n.657+107T=
ENST00000494912.5:n.1388+107T=
ENST00000498029.1:n.157+107T=
ENST00000601016.5:c.699+107T= ENSP00000469981.1:n.699+107T=
ENST00000612460.4:c.609+107T= ENSP00000481037.1:n.609+107T=
ENST00000613002.4:c.567+107T= ENSP00000478154.1:n.567+107T=
ENST00000615986.4:c.*427+107T= ENSP00000480133.1:n.*427+107T=
NM_000116.4:c.699+107T= NP_000107.1:n.699+107T=
NM_001303465.1:c.711+107T= NP_001290394.1:n.711+107T=
NM_181311.3:c.609+107T= NP_851828.1:n.609+107T=
NM_181312.3:c.657+107T= NP_851829.1:n.657+107T=
NM_181313.3:c.567+107T= NP_851830.1:n.567+107T=
NR_024048.2:n.1041+107T=
XM_006724836.1:c.753+107T= XP_006724899.1:n.753+107T=
XM_006724837.1:c.738+107T= XP_006724900.1:n.738+107T=
XM_006724839.1:c.621+107T= XP_006724902.1:n.621+107T=
XM_006724841.2:c.492+107T= XP_006724904.1:n.492+107T=
XM_006724842.2:c.402+107T= XP_006724905.1:n.402+107T=
XM_011531189.1:c.540+107T= XP_011529491.1:n.540+107T=
XM_011531190.1:c.492+107T= XP_011529492.1:n.492+107T=
XM_011531191.1:c.423+107T= XP_011529493.1:n.423+107T=
XM_011531192.1:c.420+107T= XP_011529494.1:n.420+107T=
XR_938511.1:n.1047+107T=
XM_006724841.4:c.492+107T= XP_006724904.1:n.492+107T=
XM_006724842.4:c.402+107T= XP_006724905.1:n.402+107T=
XM_011531191.2:c.423+107T= XP_011529493.1:n.423+107T=
XM_017029761.1:c.684+107T= XP_016885250.1:n.684+107T=
XM_017029762.1:c.663+107T= XP_016885251.1:n.663+107T=
XM_017029763.1:c.486+107T= XP_016885252.1:n.486+107T=
XM_017029764.1:c.420+107T= XP_016885253.1:n.420+107T=
XM_017029765.2:c.360+107T= XP_016885254.1:n.360+107T=
XM_024452431.1:c.657+107T= XP_024308199.1:n.657+107T=
NM_000116.5:c.699+107T= MANE Select NP_000107.1:n.699+107T=
NM_001303465.2:c.711+107T= NP_001290394.1:n.711+107T=
NM_181311.4:c.609+107T= NP_851828.1:n.609+107T=
NM_181312.4:c.657+107T= NP_851829.1:n.657+107T=
NM_181313.4:c.567+107T= NP_851830.1:n.567+107T=
NR_024048.3:n.1020+107T=