Canonical Allele Identifier: CA2466674917
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154412181C= , CM000685.2:g.154412181C= GRCh38
NC_000023.10:g.153640518C= , CM000685.1:g.153640518C= GRCh37
NC_000023.9:g.153293712C= NCBI36
NG_009634.1:g.5642C=
NG_012884.2:g.4908G=
NG_009634.2:g.5647C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.633C=
ENST00000698235.1:n.192C=
ENST00000698317.1:n.167C=
ENST00000698318.1:n.28C=
ENST00000475699.6:c.259C= ENSP00000419854.3:p.His87=
ENST00000476800.2:n.170C=
ENST00000483674.3:n.96C=
ENST00000601016.6:c.205C= MANE Select ENSP00000469981.1:p.His69=
ENST00000612012.5:c.205C= ENSP00000482070.2:p.His69=
ENST00000612460.5:c.205C= ENSP00000481037.1:p.His69=
ENST00000614595.2:n.563C=
ENST00000615658.5:n.518C=
ENST00000616020.5:c.259C= ENSP00000483636.2:p.His87=
ENST00000617701.5:c.205C= ENSP00000481645.1:p.His69=
ENST00000621647.2:n.258C=
ENST00000652358.1:c.-57+229C= ENSP00000498464.1:n.-57+229C=
ENST00000652390.1:c.124C= ENSP00000498858.1:p.His42=
ENST00000652476.1:n.366C=
ENST00000652682.1:c.205C= ENSP00000498288.1:p.His69=
ENST00000652685.1:n.257C=
ENST00000369776.8:c.163+175C= ENSP00000358791.4:n.163+175C=
ENST00000426231.5:c.21C=
ENST00000439735.2:c.205C= ENSP00000398193.1:p.His69=
ENST00000475699.5:c.205C= ENSP00000419854.2:p.His69=
ENST00000601016.5:c.205C= ENSP00000469981.1:p.His69=
ENST00000612012.4:c.259C= ENSP00000482070.1:p.His87=
ENST00000612460.4:c.205C= ENSP00000481037.1:p.His69=
ENST00000613002.4:c.205C= ENSP00000478154.1:p.His69=
ENST00000613634.4:n.525C=
ENST00000614595.1:n.424C=
ENST00000615658.4:n.531C=
ENST00000615986.4:c.205C= ENSP00000480133.1:p.His69=
ENST00000616020.4:c.259C= ENSP00000483636.1:p.His87=
ENST00000617701.4:c.205C= ENSP00000481645.1:p.His69=
ENST00000620808.4:c.205C= ENSP00000479311.1:p.His69=
ENST00000621647.1:n.490C=
NM_000116.4:c.205C= NP_000107.1:p.His69=
NM_001303465.1:c.259C= NP_001290394.1:p.His87=
NM_181311.3:c.205C= NP_851828.1:p.His69=
NM_181312.3:c.205C= NP_851829.1:p.His69=
NM_181313.3:c.205C= NP_851830.1:p.His69=
NR_024048.2:n.531C=
XM_006724836.1:c.259C= XP_006724899.1:p.His87=
XM_006724837.1:c.259C= XP_006724900.1:p.His87=
XM_006724839.1:c.259C= XP_006724902.1:p.His87=
XM_006724841.2:c.-90C= XP_006724904.1:n.-90C=
XM_006724842.2:c.-90C= XP_006724905.1:n.-90C=
XM_011531189.1:c.259C= XP_011529491.1:p.His87=
XR_938511.1:n.562C=
XM_006724841.4:c.-90C= XP_006724904.1:n.-90C=
XM_006724842.4:c.-90C= XP_006724905.1:n.-90C=
XM_017029761.1:c.205C= XP_016885250.1:p.His69=
XM_017029762.1:c.259C= XP_016885251.1:p.His87=
XM_017029763.1:c.205C= XP_016885252.1:p.His69=
XM_017029765.2:c.-90C= XP_016885254.1:n.-90C=
XM_024452431.1:c.259C= XP_024308199.1:p.His87=
NM_000116.5:c.205C= MANE Select NP_000107.1:p.His69=
NM_001303465.2:c.259C= NP_001290394.1:p.His87=
NM_181311.4:c.205C= NP_851828.1:p.His69=
NM_181312.4:c.205C= NP_851829.1:p.His69=
NM_181313.4:c.205C= NP_851830.1:p.His69=
NR_024048.3:n.510C=