Canonical Allele Identifier: CA2466675313
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154413400T= , CM000685.2:g.154413400T= GRCh38
NC_000023.10:g.153641737T= , CM000685.1:g.153641737T= GRCh37
NC_000023.9:g.153294931T= NCBI36
NG_009634.1:g.6861T=
NG_012884.2:g.3689A=
NG_009634.2:g.6866T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.818+42T=
ENST00000698235.1:n.358+61T=
ENST00000698317.1:n.1344+42T=
ENST00000698318.1:n.1217+30T=
ENST00000470127.2:n.481T=
ENST00000475699.6:c.339-82T= ENSP00000419854.3:n.339-82T=
ENST00000476800.2:n.1389T=
ENST00000483674.3:n.176-82T=
ENST00000601016.6:c.285-82T= MANE Select ENSP00000469981.1:n.285-82T=
ENST00000612012.5:c.285-82T= ENSP00000482070.2:n.285-82T=
ENST00000612460.5:c.285-82T= ENSP00000481037.1:n.285-82T=
ENST00000614595.2:n.1721+61T=
ENST00000615658.5:n.598-82T=
ENST00000616020.5:c.339-82T= ENSP00000483636.2:n.339-82T=
ENST00000617701.5:c.*102+42T= ENSP00000481645.1:n.*102+42T=
ENST00000621647.2:n.485T=
ENST00000652354.1:c.9-82T= ENSP00000498734.1:n.9-82T=
ENST00000652358.1:c.77+61T= ENSP00000498464.1:n.77+61T=
ENST00000652390.1:c.204-82T= ENSP00000498858.1:n.204-82T=
ENST00000652476.1:n.593T=
ENST00000652682.1:c.285-82T= ENSP00000498288.1:n.285-82T=
ENST00000652685.1:n.442+42T=
ENST00000369776.8:c.210-82T= ENSP00000358791.4:n.210-82T=
ENST00000426231.5:c.200+48T=
ENST00000439735.2:c.285-82T= ENSP00000398193.1:n.285-82T=
ENST00000475699.5:c.285-82T= ENSP00000419854.2:n.285-82T=
ENST00000476679.5:n.198-82T=
ENST00000476800.1:n.310T=
ENST00000479875.1:n.314-82T=
ENST00000483780.5:n.59-82T=
ENST00000601016.5:c.285-82T= ENSP00000469981.1:n.285-82T=
ENST00000612012.4:c.339-82T= ENSP00000482070.1:n.339-82T=
ENST00000612460.4:c.285-82T= ENSP00000481037.1:n.285-82T=
ENST00000613002.4:c.285-82T= ENSP00000478154.1:n.285-82T=
ENST00000613634.4:n.605-82T=
ENST00000615658.4:n.697+61T=
ENST00000615986.4:c.*102+42T= ENSP00000480133.1:n.*102+42T=
ENST00000616020.4:c.339-82T= ENSP00000483636.1:n.339-82T=
ENST00000617701.4:c.*114+30T= ENSP00000481645.1:n.*114+30T=
ENST00000620808.4:c.*83+61T= ENSP00000479311.1:n.*83+61T=
ENST00000621647.1:n.717T=
NM_000116.4:c.285-82T= NP_000107.1:n.285-82T=
NM_001303465.1:c.339-82T= NP_001290394.1:n.339-82T=
NM_181311.3:c.285-82T= NP_851828.1:n.285-82T=
NM_181312.3:c.285-82T= NP_851829.1:n.285-82T=
NM_181313.3:c.285-82T= NP_851830.1:n.285-82T=
NR_024048.2:n.716+42T=
XM_006724836.1:c.339-82T= XP_006724899.1:n.339-82T=
XM_006724837.1:c.339-82T= XP_006724900.1:n.339-82T=
XM_006724839.1:c.339-82T= XP_006724902.1:n.339-82T=
XM_006724841.2:c.77+61T= XP_006724904.1:n.77+61T=
XM_006724842.2:c.77+61T= XP_006724905.1:n.77+61T=
XM_011531189.1:c.339-82T= XP_011529491.1:n.339-82T=
XM_011531190.1:c.77+61T= XP_011529492.1:n.77+61T=
XM_011531191.1:c.9-82T= XP_011529493.1:n.9-82T=
XM_011531192.1:c.5+30T= XP_011529494.1:n.5+30T=
XR_938511.1:n.642-82T=
XM_006724841.4:c.77+61T= XP_006724904.1:n.77+61T=
XM_006724842.4:c.77+61T= XP_006724905.1:n.77+61T=
XM_011531191.2:c.9-82T= XP_011529493.1:n.9-82T=
XM_017029761.1:c.285-82T= XP_016885250.1:n.285-82T=
XM_017029762.1:c.339-82T= XP_016885251.1:n.339-82T=
XM_017029763.1:c.285-82T= XP_016885252.1:n.285-82T=
XM_017029764.1:c.5+30T= XP_016885253.1:n.5+30T=
XM_017029765.2:c.77+61T= XP_016885254.1:n.77+61T=
XM_024452431.1:c.339-82T= XP_024308199.1:n.339-82T=
NM_000116.5:c.285-82T= MANE Select NP_000107.1:n.285-82T=
NM_001303465.2:c.339-82T= NP_001290394.1:n.339-82T=
NM_181311.4:c.285-82T= NP_851828.1:n.285-82T=
NM_181312.4:c.285-82T= NP_851829.1:n.285-82T=
NM_181313.4:c.285-82T= NP_851830.1:n.285-82T=
NR_024048.3:n.695+42T=