Canonical Allele Identifier: CA2466677779
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420660A= , CM000685.2:g.154420660A= GRCh38
NC_000023.10:g.153648999A= , CM000685.1:g.153648999A= GRCh37
NC_000023.9:g.153302193A= NCBI36
NG_009634.1:g.14123A=
NG_009634.2:g.14126A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1512A=
ENST00000698317.1:n.2128A=
ENST00000698318.1:n.1911A=
ENST00000698319.1:n.1274A=
ENST00000698320.1:n.1162A=
ENST00000470127.2:n.1175A=
ENST00000475699.6:c.666A= ENSP00000419854.3:p.Lys222=
ENST00000483674.3:n.584A=
ENST00000601016.6:c.702A= MANE Select ENSP00000469981.1:p.Lys234=
ENST00000612012.5:c.660A= ENSP00000482070.2:p.Lys220=
ENST00000612460.5:c.612A= ENSP00000481037.1:p.Lys204=
ENST00000614595.2:n.2049A=
ENST00000615658.5:n.1291A=
ENST00000616020.5:c.714A= ENSP00000483636.2:p.Lys238=
ENST00000617701.5:c.*715A= ENSP00000481645.1:n.*715A=
ENST00000651139.1:c.-82A= ENSP00000498957.1:n.-82A=
ENST00000652354.1:c.384A= ENSP00000498734.1:p.Lys128=
ENST00000652358.1:c.495A= ENSP00000498464.1:p.Lys165=
ENST00000652390.1:c.621A= ENSP00000498858.1:p.Lys207=
ENST00000652476.1:n.1368A=
ENST00000652644.1:c.315A= ENSP00000498496.1:p.Lys105=
ENST00000652682.1:c.759A= ENSP00000498288.1:p.Lys253=
ENST00000652685.1:n.1055A=
ENST00000369776.8:c.612A= ENSP00000358791.4:p.Lys204=
ENST00000426231.5:c.699A=
ENST00000475699.5:c.660A= ENSP00000419854.2:p.Lys220=
ENST00000494912.5:n.1391A=
ENST00000498029.1:n.160A=
ENST00000601016.5:c.702A= ENSP00000469981.1:p.Lys234=
ENST00000612460.4:c.612A= ENSP00000481037.1:p.Lys204=
ENST00000613002.4:c.570A= ENSP00000478154.1:p.Lys190=
ENST00000615986.4:c.*430A= ENSP00000480133.1:n.*430A=
NM_000116.4:c.702A= NP_000107.1:p.Lys234=
NM_001303465.1:c.714A= NP_001290394.1:p.Lys238=
NM_181311.3:c.612A= NP_851828.1:p.Lys204=
NM_181312.3:c.660A= NP_851829.1:p.Lys220=
NM_181313.3:c.570A= NP_851830.1:p.Lys190=
NR_024048.2:n.1044A=
XM_006724836.1:c.756A= XP_006724899.1:p.Lys252=
XM_006724837.1:c.741A= XP_006724900.1:p.Lys247=
XM_006724839.1:c.624A= XP_006724902.1:p.Lys208=
XM_006724841.2:c.495A= XP_006724904.1:p.Lys165=
XM_006724842.2:c.405A= XP_006724905.1:p.Lys135=
XM_011531189.1:c.543A= XP_011529491.1:p.Lys181=
XM_011531190.1:c.495A= XP_011529492.1:p.Lys165=
XM_011531191.1:c.426A= XP_011529493.1:p.Lys142=
XM_011531192.1:c.423A= XP_011529494.1:p.Lys141=
XR_938511.1:n.1050A=
XM_006724841.4:c.495A= XP_006724904.1:p.Lys165=
XM_006724842.4:c.405A= XP_006724905.1:p.Lys135=
XM_011531191.2:c.426A= XP_011529493.1:p.Lys142=
XM_017029761.1:c.687A= XP_016885250.1:p.Lys229=
XM_017029762.1:c.666A= XP_016885251.1:p.Lys222=
XM_017029763.1:c.489A= XP_016885252.1:p.Lys163=
XM_017029764.1:c.423A= XP_016885253.1:p.Lys141=
XM_017029765.2:c.363A= XP_016885254.1:p.Lys121=
XM_024452431.1:c.660A= XP_024308199.1:p.Lys220=
NM_000116.5:c.702A= MANE Select NP_000107.1:p.Lys234=
NM_001303465.2:c.714A= NP_001290394.1:p.Lys238=
NM_181311.4:c.612A= NP_851828.1:p.Lys204=
NM_181312.4:c.660A= NP_851829.1:p.Lys220=
NM_181313.4:c.570A= NP_851830.1:p.Lys190=
NR_024048.3:n.1023A=