Canonical Allele Identifier: CA2466677807
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420734C= , CM000685.2:g.154420734C= GRCh38
NC_000023.10:g.153649073C= , CM000685.1:g.153649073C= GRCh37
NC_000023.9:g.153302267C= NCBI36
NG_009634.1:g.14197C=
NG_009634.2:g.14200C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1586C=
ENST00000698317.1:n.2202C=
ENST00000698318.1:n.1985C=
ENST00000698319.1:n.1348C=
ENST00000698320.1:n.1236C=
ENST00000470127.2:n.1249C=
ENST00000475699.6:c.740C= ENSP00000419854.3:p.Ala247=
ENST00000483674.3:n.658C=
ENST00000601016.6:c.776C= MANE Select ENSP00000469981.1:p.Ala259=
ENST00000612012.5:c.734C= ENSP00000482070.2:p.Ala245=
ENST00000612460.5:c.686C= ENSP00000481037.1:p.Ala229=
ENST00000614595.2:n.2123C=
ENST00000615658.5:n.1365C=
ENST00000616020.5:c.788C= ENSP00000483636.2:p.Ala263=
ENST00000617701.5:c.*789C= ENSP00000481645.1:n.*789C=
ENST00000651139.1:c.-8C= ENSP00000498957.1:n.-8C=
ENST00000652354.1:c.458C= ENSP00000498734.1:p.Ala153=
ENST00000652358.1:c.569C= ENSP00000498464.1:p.Ala190=
ENST00000652390.1:c.695C= ENSP00000498858.1:p.Ala232=
ENST00000652476.1:n.1442C=
ENST00000652644.1:c.389C= ENSP00000498496.1:p.Ala130=
ENST00000652682.1:c.833C= ENSP00000498288.1:p.Ala278=
ENST00000652685.1:n.1129C=
ENST00000369776.8:c.686C= ENSP00000358791.4:p.Ala229=
ENST00000426231.5:c.773C=
ENST00000475699.5:c.734C= ENSP00000419854.2:p.Ala245=
ENST00000494912.5:n.1465C=
ENST00000498029.1:n.234C=
ENST00000601016.5:c.776C= ENSP00000469981.1:p.Ala259=
ENST00000612460.4:c.686C= ENSP00000481037.1:p.Ala229=
ENST00000613002.4:c.644C= ENSP00000478154.1:p.Ala215=
ENST00000615986.4:c.*504C= ENSP00000480133.1:n.*504C=
NM_000116.4:c.776C= NP_000107.1:p.Ala259=
NM_001303465.1:c.788C= NP_001290394.1:p.Ala263=
NM_181311.3:c.686C= NP_851828.1:p.Ala229=
NM_181312.3:c.734C= NP_851829.1:p.Ala245=
NM_181313.3:c.644C= NP_851830.1:p.Ala215=
NR_024048.2:n.1118C=
XM_006724836.1:c.830C= XP_006724899.1:p.Ala277=
XM_006724837.1:c.815C= XP_006724900.1:p.Ala272=
XM_006724839.1:c.698C= XP_006724902.1:p.Ala233=
XM_006724841.2:c.569C= XP_006724904.1:p.Ala190=
XM_006724842.2:c.479C= XP_006724905.1:p.Ala160=
XM_011531189.1:c.617C= XP_011529491.1:p.Ala206=
XM_011531190.1:c.569C= XP_011529492.1:p.Ala190=
XM_011531191.1:c.500C= XP_011529493.1:p.Ala167=
XM_011531192.1:c.497C= XP_011529494.1:p.Ala166=
XR_938511.1:n.1124C=
XM_006724841.4:c.569C= XP_006724904.1:p.Ala190=
XM_006724842.4:c.479C= XP_006724905.1:p.Ala160=
XM_011531191.2:c.500C= XP_011529493.1:p.Ala167=
XM_017029761.1:c.761C= XP_016885250.1:p.Ala254=
XM_017029762.1:c.740C= XP_016885251.1:p.Ala247=
XM_017029763.1:c.563C= XP_016885252.1:p.Ala188=
XM_017029764.1:c.497C= XP_016885253.1:p.Ala166=
XM_017029765.2:c.437C= XP_016885254.1:p.Ala146=
XM_024452431.1:c.734C= XP_024308199.1:p.Ala245=
NM_000116.5:c.776C= MANE Select NP_000107.1:p.Ala259=
NM_001303465.2:c.788C= NP_001290394.1:p.Ala263=
NM_181311.4:c.686C= NP_851828.1:p.Ala229=
NM_181312.4:c.734C= NP_851829.1:p.Ala245=
NM_181313.4:c.644C= NP_851830.1:p.Ala215=
NR_024048.3:n.1097C=