Canonical Allele Identifier: CA2466677533
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154419935A= , CM000685.2:g.154419935A= GRCh38
NC_000023.10:g.153648274A= , CM000685.1:g.153648274A= GRCh37
NC_000023.9:g.153301468A= NCBI36
NG_009634.1:g.13398A=
NG_009634.2:g.13401A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1297A=
ENST00000698317.1:n.1913A=
ENST00000698318.1:n.1696A=
ENST00000698319.1:n.1059A=
ENST00000698320.1:n.947A=
ENST00000470127.2:n.960A=
ENST00000475699.6:c.548-97A= ENSP00000419854.3:n.548-97A=
ENST00000483674.3:n.466-97A=
ENST00000601016.6:c.584-97A= MANE Select ENSP00000469981.1:n.584-97A=
ENST00000612012.5:c.542-97A= ENSP00000482070.2:n.542-97A=
ENST00000612460.5:c.494-97A= ENSP00000481037.1:n.494-97A=
ENST00000614595.2:n.1931-97A=
ENST00000615658.5:n.1076A=
ENST00000616020.5:c.596-97A= ENSP00000483636.2:n.596-97A=
ENST00000617701.5:c.*500A= ENSP00000481645.1:n.*500A=
ENST00000652354.1:c.266-97A= ENSP00000498734.1:n.266-97A=
ENST00000652358.1:c.377-97A= ENSP00000498464.1:n.377-97A=
ENST00000652390.1:c.503-97A= ENSP00000498858.1:n.503-97A=
ENST00000652476.1:n.1153A=
ENST00000652644.1:c.197-97A= ENSP00000498496.1:n.197-97A=
ENST00000652682.1:c.641-97A= ENSP00000498288.1:n.641-97A=
ENST00000652685.1:n.840A=
ENST00000369776.8:c.377-97A= ENSP00000358791.4:n.377-97A=
ENST00000426231.5:c.581-97A=
ENST00000439735.2:c.491-97A= ENSP00000398193.1:n.491-97A=
ENST00000470127.1:n.163-97A=
ENST00000475699.5:c.542-97A= ENSP00000419854.2:n.542-97A=
ENST00000476679.5:n.766A=
ENST00000494912.5:n.1273-97A=
ENST00000601016.5:c.584-97A= ENSP00000469981.1:n.584-97A=
ENST00000612012.4:c.548-97A= ENSP00000482070.1:n.548-97A=
ENST00000612460.4:c.494-97A= ENSP00000481037.1:n.494-97A=
ENST00000613002.4:c.452-97A= ENSP00000478154.1:n.452-97A=
ENST00000613634.4:n.1002A=
ENST00000615658.4:n.1176A=
ENST00000615986.4:c.*312-97A= ENSP00000480133.1:n.*312-97A=
ENST00000620808.4:c.*170-97A= ENSP00000479311.1:n.*170-97A=
NM_000116.4:c.584-97A= NP_000107.1:n.584-97A=
NM_001303465.1:c.596-97A= NP_001290394.1:n.596-97A=
NM_181311.3:c.494-97A= NP_851828.1:n.494-97A=
NM_181312.3:c.542-97A= NP_851829.1:n.542-97A=
NM_181313.3:c.452-97A= NP_851830.1:n.452-97A=
NR_024048.2:n.926-97A=
XM_006724836.1:c.638-97A= XP_006724899.1:n.638-97A=
XM_006724837.1:c.506-97A= XP_006724900.1:n.506-97A=
XM_006724839.1:c.506-97A= XP_006724902.1:n.506-97A=
XM_006724841.2:c.377-97A= XP_006724904.1:n.377-97A=
XM_006724842.2:c.287-97A= XP_006724905.1:n.287-97A=
XM_011531189.1:c.425-97A= XP_011529491.1:n.425-97A=
XM_011531190.1:c.377-97A= XP_011529492.1:n.377-97A=
XM_011531191.1:c.308-97A= XP_011529493.1:n.308-97A=
XM_011531192.1:c.305-97A= XP_011529494.1:n.305-97A=
XR_938511.1:n.932-97A=
XM_006724841.4:c.377-97A= XP_006724904.1:n.377-97A=
XM_006724842.4:c.287-97A= XP_006724905.1:n.287-97A=
XM_011531191.2:c.308-97A= XP_011529493.1:n.308-97A=
XM_017029761.1:c.452-97A= XP_016885250.1:n.452-97A=
XM_017029762.1:c.548-97A= XP_016885251.1:n.548-97A=
XM_017029763.1:c.371-97A= XP_016885252.1:n.371-97A=
XM_017029764.1:c.305-97A= XP_016885253.1:n.305-97A=
XM_017029765.2:c.245-97A= XP_016885254.1:n.245-97A=
XM_024452431.1:c.425-97A= XP_024308199.1:n.425-97A=
NM_000116.5:c.584-97A= MANE Select NP_000107.1:n.584-97A=
NM_001303465.2:c.596-97A= NP_001290394.1:n.596-97A=
NM_181311.4:c.494-97A= NP_851828.1:n.494-97A=
NM_181312.4:c.542-97A= NP_851829.1:n.542-97A=
NM_181313.4:c.452-97A= NP_851830.1:n.452-97A=
NR_024048.3:n.905-97A=