Canonical Allele Identifier: CA2466675252
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154413236C= , CM000685.2:g.154413236C= GRCh38
NC_000023.10:g.153641573C= , CM000685.1:g.153641573C= GRCh37
NC_000023.9:g.153294767C= NCBI36
NG_009634.1:g.6697C=
NG_012884.2:g.3853G=
NG_009634.2:g.6702C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.696C=
ENST00000698235.1:n.255C=
ENST00000698317.1:n.1222C=
ENST00000698318.1:n.1083C=
ENST00000470127.2:n.317C=
ENST00000475699.6:c.322C= ENSP00000419854.3:p.Leu108=
ENST00000476800.2:n.1225C=
ENST00000483674.3:n.159C=
ENST00000601016.6:c.268C= MANE Select ENSP00000469981.1:p.Leu90=
ENST00000612012.5:c.268C= ENSP00000482070.2:p.Leu90=
ENST00000612460.5:c.268C= ENSP00000481037.1:p.Leu90=
ENST00000614595.2:n.1618C=
ENST00000615658.5:n.581C=
ENST00000616020.5:c.322C= ENSP00000483636.2:p.Leu108=
ENST00000617701.5:c.268C= ENSP00000481645.1:p.Leu90=
ENST00000621647.2:n.321C=
ENST00000652354.1:c.-9C= ENSP00000498734.1:n.-9C=
ENST00000652358.1:c.-27C= ENSP00000498464.1:n.-27C=
ENST00000652390.1:c.187C= ENSP00000498858.1:p.Leu63=
ENST00000652476.1:n.429C=
ENST00000652682.1:c.268C= ENSP00000498288.1:p.Leu90=
ENST00000652685.1:n.320C=
ENST00000369776.8:c.193C= ENSP00000358791.4:p.Leu65=
ENST00000426231.5:c.84C=
ENST00000439735.2:c.268C= ENSP00000398193.1:p.Leu90=
ENST00000475699.5:c.268C= ENSP00000419854.2:p.Leu90=
ENST00000476679.5:n.181C=
ENST00000476800.1:n.146C=
ENST00000479875.1:n.297C=
ENST00000483780.5:n.42C=
ENST00000601016.5:c.268C= ENSP00000469981.1:p.Leu90=
ENST00000612012.4:c.322C= ENSP00000482070.1:p.Leu108=
ENST00000612460.4:c.268C= ENSP00000481037.1:p.Leu90=
ENST00000613002.4:c.268C= ENSP00000478154.1:p.Leu90=
ENST00000613634.4:n.588C=
ENST00000615658.4:n.594C=
ENST00000615986.4:c.268C= ENSP00000480133.1:p.Leu90=
ENST00000616020.4:c.322C= ENSP00000483636.1:p.Leu108=
ENST00000617701.4:c.268C= ENSP00000481645.1:p.Leu90=
ENST00000620808.4:c.268C= ENSP00000479311.1:p.Leu90=
ENST00000621647.1:n.553C=
NM_000116.4:c.268C= NP_000107.1:p.Leu90=
NM_001303465.1:c.322C= NP_001290394.1:p.Leu108=
NM_181311.3:c.268C= NP_851828.1:p.Leu90=
NM_181312.3:c.268C= NP_851829.1:p.Leu90=
NM_181313.3:c.268C= NP_851830.1:p.Leu90=
NR_024048.2:n.594C=
XM_006724836.1:c.322C= XP_006724899.1:p.Leu108=
XM_006724837.1:c.322C= XP_006724900.1:p.Leu108=
XM_006724839.1:c.322C= XP_006724902.1:p.Leu108=
XM_006724841.2:c.-27C= XP_006724904.1:n.-27C=
XM_006724842.2:c.-27C= XP_006724905.1:n.-27C=
XM_011531189.1:c.322C= XP_011529491.1:p.Leu108=
XM_011531190.1:c.-27C= XP_011529492.1:n.-27C=
XM_011531191.1:c.-9C= XP_011529493.1:n.-9C=
XM_011531192.1:c.-130C= XP_011529494.1:n.-130C=
XR_938511.1:n.625C=
XM_006724841.4:c.-27C= XP_006724904.1:n.-27C=
XM_006724842.4:c.-27C= XP_006724905.1:n.-27C=
XM_011531191.2:c.-9C= XP_011529493.1:n.-9C=
XM_017029761.1:c.268C= XP_016885250.1:p.Leu90=
XM_017029762.1:c.322C= XP_016885251.1:p.Leu108=
XM_017029763.1:c.268C= XP_016885252.1:p.Leu90=
XM_017029764.1:c.-130C= XP_016885253.1:n.-130C=
XM_017029765.2:c.-27C= XP_016885254.1:n.-27C=
XM_024452431.1:c.322C= XP_024308199.1:p.Leu108=
NM_000116.5:c.268C= MANE Select NP_000107.1:p.Leu90=
NM_001303465.2:c.322C= NP_001290394.1:p.Leu108=
NM_181311.4:c.268C= NP_851828.1:p.Leu90=
NM_181312.4:c.268C= NP_851829.1:p.Leu90=
NM_181313.4:c.268C= NP_851830.1:p.Leu90=
NR_024048.3:n.573C=