Canonical Allele Identifier: CA2466677800
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420719C= , CM000685.2:g.154420719C= GRCh38
NC_000023.10:g.153649058C= , CM000685.1:g.153649058C= GRCh37
NC_000023.9:g.153302252C= NCBI36
NG_009634.1:g.14182C=
NG_009634.2:g.14185C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1571C=
ENST00000698317.1:n.2187C=
ENST00000698318.1:n.1970C=
ENST00000698319.1:n.1333C=
ENST00000698320.1:n.1221C=
ENST00000470127.2:n.1234C=
ENST00000475699.6:c.725C= ENSP00000419854.3:p.Ala242=
ENST00000483674.3:n.643C=
ENST00000601016.6:c.761C= MANE Select ENSP00000469981.1:p.Ala254=
ENST00000612012.5:c.719C= ENSP00000482070.2:p.Ala240=
ENST00000612460.5:c.671C= ENSP00000481037.1:p.Ala224=
ENST00000614595.2:n.2108C=
ENST00000615658.5:n.1350C=
ENST00000616020.5:c.773C= ENSP00000483636.2:p.Ala258=
ENST00000617701.5:c.*774C= ENSP00000481645.1:n.*774C=
ENST00000651139.1:c.-23C= ENSP00000498957.1:n.-23C=
ENST00000652354.1:c.443C= ENSP00000498734.1:p.Ala148=
ENST00000652358.1:c.554C= ENSP00000498464.1:p.Ala185=
ENST00000652390.1:c.680C= ENSP00000498858.1:p.Ala227=
ENST00000652476.1:n.1427C=
ENST00000652644.1:c.374C= ENSP00000498496.1:p.Ala125=
ENST00000652682.1:c.818C= ENSP00000498288.1:p.Ala273=
ENST00000652685.1:n.1114C=
ENST00000369776.8:c.671C= ENSP00000358791.4:p.Ala224=
ENST00000426231.5:c.758C=
ENST00000475699.5:c.719C= ENSP00000419854.2:p.Ala240=
ENST00000494912.5:n.1450C=
ENST00000498029.1:n.219C=
ENST00000601016.5:c.761C= ENSP00000469981.1:p.Ala254=
ENST00000612460.4:c.671C= ENSP00000481037.1:p.Ala224=
ENST00000613002.4:c.629C= ENSP00000478154.1:p.Ala210=
ENST00000615986.4:c.*489C= ENSP00000480133.1:n.*489C=
NM_000116.4:c.761C= NP_000107.1:p.Ala254=
NM_001303465.1:c.773C= NP_001290394.1:p.Ala258=
NM_181311.3:c.671C= NP_851828.1:p.Ala224=
NM_181312.3:c.719C= NP_851829.1:p.Ala240=
NM_181313.3:c.629C= NP_851830.1:p.Ala210=
NR_024048.2:n.1103C=
XM_006724836.1:c.815C= XP_006724899.1:p.Ala272=
XM_006724837.1:c.800C= XP_006724900.1:p.Ala267=
XM_006724839.1:c.683C= XP_006724902.1:p.Ala228=
XM_006724841.2:c.554C= XP_006724904.1:p.Ala185=
XM_006724842.2:c.464C= XP_006724905.1:p.Ala155=
XM_011531189.1:c.602C= XP_011529491.1:p.Ala201=
XM_011531190.1:c.554C= XP_011529492.1:p.Ala185=
XM_011531191.1:c.485C= XP_011529493.1:p.Ala162=
XM_011531192.1:c.482C= XP_011529494.1:p.Ala161=
XR_938511.1:n.1109C=
XM_006724841.4:c.554C= XP_006724904.1:p.Ala185=
XM_006724842.4:c.464C= XP_006724905.1:p.Ala155=
XM_011531191.2:c.485C= XP_011529493.1:p.Ala162=
XM_017029761.1:c.746C= XP_016885250.1:p.Ala249=
XM_017029762.1:c.725C= XP_016885251.1:p.Ala242=
XM_017029763.1:c.548C= XP_016885252.1:p.Ala183=
XM_017029764.1:c.482C= XP_016885253.1:p.Ala161=
XM_017029765.2:c.422C= XP_016885254.1:p.Ala141=
XM_024452431.1:c.719C= XP_024308199.1:p.Ala240=
NM_000116.5:c.761C= MANE Select NP_000107.1:p.Ala254=
NM_001303465.2:c.773C= NP_001290394.1:p.Ala258=
NM_181311.4:c.671C= NP_851828.1:p.Ala224=
NM_181312.4:c.719C= NP_851829.1:p.Ala240=
NM_181313.4:c.629C= NP_851830.1:p.Ala210=
NR_024048.3:n.1082C=