Canonical Allele Identifier: CA2466677803
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420726C= , CM000685.2:g.154420726C= GRCh38
NC_000023.10:g.153649065C= , CM000685.1:g.153649065C= GRCh37
NC_000023.9:g.153302259C= NCBI36
NG_009634.1:g.14189C=
NG_009634.2:g.14192C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1578C=
ENST00000698317.1:n.2194C=
ENST00000698318.1:n.1977C=
ENST00000698319.1:n.1340C=
ENST00000698320.1:n.1228C=
ENST00000470127.2:n.1241C=
ENST00000475699.6:c.732C= ENSP00000419854.3:p.Asn244=
ENST00000483674.3:n.650C=
ENST00000601016.6:c.768C= MANE Select ENSP00000469981.1:p.Asn256=
ENST00000612012.5:c.726C= ENSP00000482070.2:p.Asn242=
ENST00000612460.5:c.678C= ENSP00000481037.1:p.Asn226=
ENST00000614595.2:n.2115C=
ENST00000615658.5:n.1357C=
ENST00000616020.5:c.780C= ENSP00000483636.2:p.Asn260=
ENST00000617701.5:c.*781C= ENSP00000481645.1:n.*781C=
ENST00000651139.1:c.-16C= ENSP00000498957.1:n.-16C=
ENST00000652354.1:c.450C= ENSP00000498734.1:p.Asn150=
ENST00000652358.1:c.561C= ENSP00000498464.1:p.Asn187=
ENST00000652390.1:c.687C= ENSP00000498858.1:p.Asn229=
ENST00000652476.1:n.1434C=
ENST00000652644.1:c.381C= ENSP00000498496.1:p.Asn127=
ENST00000652682.1:c.825C= ENSP00000498288.1:p.Asn275=
ENST00000652685.1:n.1121C=
ENST00000369776.8:c.678C= ENSP00000358791.4:p.Asn226=
ENST00000426231.5:c.765C=
ENST00000475699.5:c.726C= ENSP00000419854.2:p.Asn242=
ENST00000494912.5:n.1457C=
ENST00000498029.1:n.226C=
ENST00000601016.5:c.768C= ENSP00000469981.1:p.Asn256=
ENST00000612460.4:c.678C= ENSP00000481037.1:p.Asn226=
ENST00000613002.4:c.636C= ENSP00000478154.1:p.Asn212=
ENST00000615986.4:c.*496C= ENSP00000480133.1:n.*496C=
NM_000116.4:c.768C= NP_000107.1:p.Asn256=
NM_001303465.1:c.780C= NP_001290394.1:p.Asn260=
NM_181311.3:c.678C= NP_851828.1:p.Asn226=
NM_181312.3:c.726C= NP_851829.1:p.Asn242=
NM_181313.3:c.636C= NP_851830.1:p.Asn212=
NR_024048.2:n.1110C=
XM_006724836.1:c.822C= XP_006724899.1:p.Asn274=
XM_006724837.1:c.807C= XP_006724900.1:p.Asn269=
XM_006724839.1:c.690C= XP_006724902.1:p.Asn230=
XM_006724841.2:c.561C= XP_006724904.1:p.Asn187=
XM_006724842.2:c.471C= XP_006724905.1:p.Asn157=
XM_011531189.1:c.609C= XP_011529491.1:p.Asn203=
XM_011531190.1:c.561C= XP_011529492.1:p.Asn187=
XM_011531191.1:c.492C= XP_011529493.1:p.Asn164=
XM_011531192.1:c.489C= XP_011529494.1:p.Asn163=
XR_938511.1:n.1116C=
XM_006724841.4:c.561C= XP_006724904.1:p.Asn187=
XM_006724842.4:c.471C= XP_006724905.1:p.Asn157=
XM_011531191.2:c.492C= XP_011529493.1:p.Asn164=
XM_017029761.1:c.753C= XP_016885250.1:p.Asn251=
XM_017029762.1:c.732C= XP_016885251.1:p.Asn244=
XM_017029763.1:c.555C= XP_016885252.1:p.Asn185=
XM_017029764.1:c.489C= XP_016885253.1:p.Asn163=
XM_017029765.2:c.429C= XP_016885254.1:p.Asn143=
XM_024452431.1:c.726C= XP_024308199.1:p.Asn242=
NM_000116.5:c.768C= MANE Select NP_000107.1:p.Asn256=
NM_001303465.2:c.780C= NP_001290394.1:p.Asn260=
NM_181311.4:c.678C= NP_851828.1:p.Asn226=
NM_181312.4:c.726C= NP_851829.1:p.Asn242=
NM_181313.4:c.636C= NP_851830.1:p.Asn212=
NR_024048.3:n.1089C=