Canonical Allele Identifier: CA2466677798
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420715C= , CM000685.2:g.154420715C= GRCh38
NC_000023.10:g.153649054C= , CM000685.1:g.153649054C= GRCh37
NC_000023.9:g.153302248C= NCBI36
NG_009634.1:g.14178C=
NG_009634.2:g.14181C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1567C=
ENST00000698317.1:n.2183C=
ENST00000698318.1:n.1966C=
ENST00000698319.1:n.1329C=
ENST00000698320.1:n.1217C=
ENST00000470127.2:n.1230C=
ENST00000475699.6:c.721C= ENSP00000419854.3:p.Arg241=
ENST00000483674.3:n.639C=
ENST00000601016.6:c.757C= MANE Select ENSP00000469981.1:p.Arg253=
ENST00000612012.5:c.715C= ENSP00000482070.2:p.Arg239=
ENST00000612460.5:c.667C= ENSP00000481037.1:p.Arg223=
ENST00000614595.2:n.2104C=
ENST00000615658.5:n.1346C=
ENST00000616020.5:c.769C= ENSP00000483636.2:p.Arg257=
ENST00000617701.5:c.*770C= ENSP00000481645.1:n.*770C=
ENST00000651139.1:c.-27C= ENSP00000498957.1:n.-27C=
ENST00000652354.1:c.439C= ENSP00000498734.1:p.Arg147=
ENST00000652358.1:c.550C= ENSP00000498464.1:p.Arg184=
ENST00000652390.1:c.676C= ENSP00000498858.1:p.Arg226=
ENST00000652476.1:n.1423C=
ENST00000652644.1:c.370C= ENSP00000498496.1:p.Arg124=
ENST00000652682.1:c.814C= ENSP00000498288.1:p.Arg272=
ENST00000652685.1:n.1110C=
ENST00000369776.8:c.667C= ENSP00000358791.4:p.Arg223=
ENST00000426231.5:c.754C=
ENST00000475699.5:c.715C= ENSP00000419854.2:p.Arg239=
ENST00000494912.5:n.1446C=
ENST00000498029.1:n.215C=
ENST00000601016.5:c.757C= ENSP00000469981.1:p.Arg253=
ENST00000612460.4:c.667C= ENSP00000481037.1:p.Arg223=
ENST00000613002.4:c.625C= ENSP00000478154.1:p.Arg209=
ENST00000615986.4:c.*485C= ENSP00000480133.1:n.*485C=
NM_000116.4:c.757C= NP_000107.1:p.Arg253=
NM_001303465.1:c.769C= NP_001290394.1:p.Arg257=
NM_181311.3:c.667C= NP_851828.1:p.Arg223=
NM_181312.3:c.715C= NP_851829.1:p.Arg239=
NM_181313.3:c.625C= NP_851830.1:p.Arg209=
NR_024048.2:n.1099C=
XM_006724836.1:c.811C= XP_006724899.1:p.Arg271=
XM_006724837.1:c.796C= XP_006724900.1:p.Arg266=
XM_006724839.1:c.679C= XP_006724902.1:p.Arg227=
XM_006724841.2:c.550C= XP_006724904.1:p.Arg184=
XM_006724842.2:c.460C= XP_006724905.1:p.Arg154=
XM_011531189.1:c.598C= XP_011529491.1:p.Arg200=
XM_011531190.1:c.550C= XP_011529492.1:p.Arg184=
XM_011531191.1:c.481C= XP_011529493.1:p.Arg161=
XM_011531192.1:c.478C= XP_011529494.1:p.Arg160=
XR_938511.1:n.1105C=
XM_006724841.4:c.550C= XP_006724904.1:p.Arg184=
XM_006724842.4:c.460C= XP_006724905.1:p.Arg154=
XM_011531191.2:c.481C= XP_011529493.1:p.Arg161=
XM_017029761.1:c.742C= XP_016885250.1:p.Arg248=
XM_017029762.1:c.721C= XP_016885251.1:p.Arg241=
XM_017029763.1:c.544C= XP_016885252.1:p.Arg182=
XM_017029764.1:c.478C= XP_016885253.1:p.Arg160=
XM_017029765.2:c.418C= XP_016885254.1:p.Arg140=
XM_024452431.1:c.715C= XP_024308199.1:p.Arg239=
NM_000116.5:c.757C= MANE Select NP_000107.1:p.Arg253=
NM_001303465.2:c.769C= NP_001290394.1:p.Arg257=
NM_181311.4:c.667C= NP_851828.1:p.Arg223=
NM_181312.4:c.715C= NP_851829.1:p.Arg239=
NM_181313.4:c.625C= NP_851830.1:p.Arg209=
NR_024048.3:n.1078C=