Canonical Allele Identifier: CA2466677537
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154419949G= , CM000685.2:g.154419949G= GRCh38
NC_000023.10:g.153648288G= , CM000685.1:g.153648288G= GRCh37
NC_000023.9:g.153301482G= NCBI36
NG_009634.1:g.13412G=
NG_009634.2:g.13415G=

Transcript Alleles

HGVS Amino-acid change
ENST00000698234.1:n.1311G=
ENST00000698317.1:n.1927G=
ENST00000698318.1:n.1710G=
ENST00000698319.1:n.1073G=
ENST00000698320.1:n.961G=
ENST00000470127.2:n.974G=
ENST00000475699.6:c.548-83G= ENSP00000419854.3:n.548-83G=
ENST00000483674.3:n.466-83G=
ENST00000601016.6:c.584-83G= MANE Select ENSP00000469981.1:n.584-83G=
ENST00000612012.5:c.542-83G= ENSP00000482070.2:n.542-83G=
ENST00000612460.5:c.494-83G= ENSP00000481037.1:n.494-83G=
ENST00000614595.2:n.1931-83G=
ENST00000615658.5:n.1090G=
ENST00000616020.5:c.596-83G= ENSP00000483636.2:n.596-83G=
ENST00000617701.5:c.*514G= ENSP00000481645.1:n.*514G=
ENST00000652354.1:c.266-83G= ENSP00000498734.1:n.266-83G=
ENST00000652358.1:c.377-83G= ENSP00000498464.1:n.377-83G=
ENST00000652390.1:c.503-83G= ENSP00000498858.1:n.503-83G=
ENST00000652476.1:n.1167G=
ENST00000652644.1:c.197-83G= ENSP00000498496.1:n.197-83G=
ENST00000652682.1:c.641-83G= ENSP00000498288.1:n.641-83G=
ENST00000652685.1:n.854G=
ENST00000369776.8:c.377-83G= ENSP00000358791.4:n.377-83G=
ENST00000426231.5:c.581-83G=
ENST00000439735.2:c.491-83G= ENSP00000398193.1:n.491-83G=
ENST00000470127.1:n.163-83G=
ENST00000475699.5:c.542-83G= ENSP00000419854.2:n.542-83G=
ENST00000476679.5:n.780G=
ENST00000494912.5:n.1273-83G=
ENST00000601016.5:c.584-83G= ENSP00000469981.1:n.584-83G=
ENST00000612012.4:c.548-83G= ENSP00000482070.1:n.548-83G=
ENST00000612460.4:c.494-83G= ENSP00000481037.1:n.494-83G=
ENST00000613002.4:c.452-83G= ENSP00000478154.1:n.452-83G=
ENST00000613634.4:n.1016G=
ENST00000615658.4:n.1190G=
ENST00000615986.4:c.*312-83G= ENSP00000480133.1:n.*312-83G=
ENST00000620808.4:c.*170-83G= ENSP00000479311.1:n.*170-83G=
NM_000116.4:c.584-83G= NP_000107.1:n.584-83G=
NM_001303465.1:c.596-83G= NP_001290394.1:n.596-83G=
NM_181311.3:c.494-83G= NP_851828.1:n.494-83G=
NM_181312.3:c.542-83G= NP_851829.1:n.542-83G=
NM_181313.3:c.452-83G= NP_851830.1:n.452-83G=
NR_024048.2:n.926-83G=
XM_006724836.1:c.638-83G= XP_006724899.1:n.638-83G=
XM_006724837.1:c.506-83G= XP_006724900.1:n.506-83G=
XM_006724839.1:c.506-83G= XP_006724902.1:n.506-83G=
XM_006724841.2:c.377-83G= XP_006724904.1:n.377-83G=
XM_006724842.2:c.287-83G= XP_006724905.1:n.287-83G=
XM_011531189.1:c.425-83G= XP_011529491.1:n.425-83G=
XM_011531190.1:c.377-83G= XP_011529492.1:n.377-83G=
XM_011531191.1:c.308-83G= XP_011529493.1:n.308-83G=
XM_011531192.1:c.305-83G= XP_011529494.1:n.305-83G=
XR_938511.1:n.932-83G=
XM_006724841.4:c.377-83G= XP_006724904.1:n.377-83G=
XM_006724842.4:c.287-83G= XP_006724905.1:n.287-83G=
XM_011531191.2:c.308-83G= XP_011529493.1:n.308-83G=
XM_017029761.1:c.452-83G= XP_016885250.1:n.452-83G=
XM_017029762.1:c.548-83G= XP_016885251.1:n.548-83G=
XM_017029763.1:c.371-83G= XP_016885252.1:n.371-83G=
XM_017029764.1:c.305-83G= XP_016885253.1:n.305-83G=
XM_017029765.2:c.245-83G= XP_016885254.1:n.245-83G=
XM_024452431.1:c.425-83G= XP_024308199.1:n.425-83G=
NM_000116.5:c.584-83G= MANE Select NP_000107.1:n.584-83G=
NM_001303465.2:c.596-83G= NP_001290394.1:n.596-83G=
NM_181311.4:c.494-83G= NP_851828.1:n.494-83G=
NM_181312.4:c.542-83G= NP_851829.1:n.542-83G=
NM_181313.4:c.452-83G= NP_851830.1:n.452-83G=
NR_024048.3:n.905-83G=