Canonical Allele Identifier: CA2466677502
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154419864C= , CM000685.2:g.154419864C= GRCh38
NC_000023.10:g.153648203C= , CM000685.1:g.153648203C= GRCh37
NC_000023.9:g.153301397C= NCBI36
NG_009634.1:g.13327C=
NG_009634.2:g.13330C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1226C=
ENST00000698317.1:n.1842C=
ENST00000698318.1:n.1625C=
ENST00000698319.1:n.988C=
ENST00000698320.1:n.876C=
ENST00000470127.2:n.889C=
ENST00000475699.6:c.547+118C= ENSP00000419854.3:n.547+118C=
ENST00000483674.3:n.465+118C=
ENST00000601016.6:c.583+118C= MANE Select ENSP00000469981.1:n.583+118C=
ENST00000612012.5:c.542-168C= ENSP00000482070.2:n.542-168C=
ENST00000612460.5:c.493+118C= ENSP00000481037.1:n.493+118C=
ENST00000614595.2:n.1930+118C=
ENST00000615658.5:n.1005C=
ENST00000616020.5:c.596-168C= ENSP00000483636.2:n.596-168C=
ENST00000617701.5:c.*429C= ENSP00000481645.1:n.*429C=
ENST00000652354.1:c.266-168C= ENSP00000498734.1:n.266-168C=
ENST00000652358.1:c.376+118C= ENSP00000498464.1:n.376+118C=
ENST00000652390.1:c.502+118C= ENSP00000498858.1:n.502+118C=
ENST00000652476.1:n.1082C=
ENST00000652644.1:c.196+118C= ENSP00000498496.1:n.196+118C=
ENST00000652682.1:c.640+118C= ENSP00000498288.1:n.640+118C=
ENST00000652685.1:n.769C=
ENST00000369776.8:c.377-168C= ENSP00000358791.4:n.377-168C=
ENST00000426231.5:c.580+118C=
ENST00000439735.2:c.490+118C= ENSP00000398193.1:n.490+118C=
ENST00000470127.1:n.162+118C=
ENST00000475699.5:c.542-168C= ENSP00000419854.2:n.542-168C=
ENST00000476679.5:n.695C=
ENST00000494912.5:n.1272+118C=
ENST00000601016.5:c.583+118C= ENSP00000469981.1:n.583+118C=
ENST00000612012.4:c.547+118C= ENSP00000482070.1:n.547+118C=
ENST00000612460.4:c.493+118C= ENSP00000481037.1:n.493+118C=
ENST00000613002.4:c.452-168C= ENSP00000478154.1:n.452-168C=
ENST00000613634.4:n.931C=
ENST00000615658.4:n.1105C=
ENST00000615986.4:c.*311+118C= ENSP00000480133.1:n.*311+118C=
ENST00000620808.4:c.*170-168C= ENSP00000479311.1:n.*170-168C=
NM_000116.4:c.583+118C= NP_000107.1:n.583+118C=
NM_001303465.1:c.596-168C= NP_001290394.1:n.596-168C=
NM_181311.3:c.493+118C= NP_851828.1:n.493+118C=
NM_181312.3:c.542-168C= NP_851829.1:n.542-168C=
NM_181313.3:c.452-168C= NP_851830.1:n.452-168C=
NR_024048.2:n.925+118C=
XM_006724836.1:c.637+118C= XP_006724899.1:n.637+118C=
XM_006724837.1:c.506-168C= XP_006724900.1:n.506-168C=
XM_006724839.1:c.506-168C= XP_006724902.1:n.506-168C=
XM_006724841.2:c.376+118C= XP_006724904.1:n.376+118C=
XM_006724842.2:c.286+118C= XP_006724905.1:n.286+118C=
XM_011531189.1:c.425-168C= XP_011529491.1:n.425-168C=
XM_011531190.1:c.376+118C= XP_011529492.1:n.376+118C=
XM_011531191.1:c.307+118C= XP_011529493.1:n.307+118C=
XM_011531192.1:c.304+118C= XP_011529494.1:n.304+118C=
XR_938511.1:n.931+118C=
XM_006724841.4:c.376+118C= XP_006724904.1:n.376+118C=
XM_006724842.4:c.286+118C= XP_006724905.1:n.286+118C=
XM_011531191.2:c.307+118C= XP_011529493.1:n.307+118C=
XM_017029761.1:c.452-168C= XP_016885250.1:n.452-168C=
XM_017029762.1:c.547+118C= XP_016885251.1:n.547+118C=
XM_017029763.1:c.371-168C= XP_016885252.1:n.371-168C=
XM_017029764.1:c.304+118C= XP_016885253.1:n.304+118C=
XM_017029765.2:c.245-168C= XP_016885254.1:n.245-168C=
XM_024452431.1:c.425-168C= XP_024308199.1:n.425-168C=
NM_000116.5:c.583+118C= MANE Select NP_000107.1:n.583+118C=
NM_001303465.2:c.596-168C= NP_001290394.1:n.596-168C=
NM_181311.4:c.493+118C= NP_851828.1:n.493+118C=
NM_181312.4:c.542-168C= NP_851829.1:n.542-168C=
NM_181313.4:c.452-168C= NP_851830.1:n.452-168C=
NR_024048.3:n.904+118C=