Canonical Allele Identifier: CA2695120729

Gene: TAFAZZIN

Linked Data

• gnomAD v4: X-154412456-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154412456A>G , CM000685.2:g.154412456A>G	GRCh38
NC_000023.10:g.153640793A>G , CM000685.1:g.153640793A>G	GRCh37
NC_000023.9:g.153293987A>G	NCBI36
NG_009634.1:g.5917A>G
NG_012884.2:g.4633T>C
NG_009634.2:g.5922A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.666+242A>G
ENST00000698235.1:n.225+242A>G
ENST00000698317.1:n.442A>G
ENST00000698318.1:n.303A>G
ENST00000475699.6:c.292+242A>G	ENSP00000419854.3:n.292+242A>G
ENST00000476800.2:n.445A>G
ENST00000483674.3:n.129+242A>G
ENST00000601016.6:c.238+242A>G MANE Select	ENSP00000469981.1:n.238+242A>G
ENST00000612012.5:c.238+242A>G	ENSP00000482070.2:n.238+242A>G
ENST00000612460.5:c.238+242A>G	ENSP00000481037.1:n.238+242A>G
ENST00000614595.2:n.838A>G
ENST00000615658.5:n.551+242A>G
ENST00000616020.5:c.292+242A>G	ENSP00000483636.2:n.292+242A>G
ENST00000617701.5:c.238+242A>G	ENSP00000481645.1:n.238+242A>G
ENST00000621647.2:n.291+242A>G
ENST00000652358.1:c.-57+504A>G	ENSP00000498464.1:n.-57+504A>G
ENST00000652390.1:c.157+242A>G	ENSP00000498858.1:n.157+242A>G
ENST00000652476.1:n.399+242A>G
ENST00000652682.1:c.238+242A>G	ENSP00000498288.1:n.238+242A>G
ENST00000652685.1:n.290+242A>G
ENST00000369776.8:c.163+450A>G	ENSP00000358791.4:n.163+450A>G
ENST00000426231.5:c.54+242A>G
ENST00000439735.2:c.238+242A>G	ENSP00000398193.1:n.238+242A>G
ENST00000475699.5:c.238+242A>G	ENSP00000419854.2:n.238+242A>G
ENST00000483780.5:n.12+242A>G
ENST00000601016.5:c.238+242A>G	ENSP00000469981.1:n.238+242A>G
ENST00000612012.4:c.292+242A>G	ENSP00000482070.1:n.292+242A>G
ENST00000612460.4:c.238+242A>G	ENSP00000481037.1:n.238+242A>G
ENST00000613002.4:c.238+242A>G	ENSP00000478154.1:n.238+242A>G
ENST00000613634.4:n.558+242A>G
ENST00000614595.1:n.699A>G
ENST00000615658.4:n.564+242A>G
ENST00000615986.4:c.238+242A>G	ENSP00000480133.1:n.238+242A>G
ENST00000616020.4:c.292+242A>G	ENSP00000483636.1:n.292+242A>G
ENST00000617701.4:c.238+242A>G	ENSP00000481645.1:n.238+242A>G
ENST00000620808.4:c.238+242A>G	ENSP00000479311.1:n.238+242A>G
ENST00000621647.1:n.523+242A>G
NM_000116.4:c.238+242A>G	NP_000107.1:n.238+242A>G
NM_001303465.1:c.292+242A>G	NP_001290394.1:n.292+242A>G
NM_181311.3:c.238+242A>G	NP_851828.1:n.238+242A>G
NM_181312.3:c.238+242A>G	NP_851829.1:n.238+242A>G
NM_181313.3:c.238+242A>G	NP_851830.1:n.238+242A>G
NR_024048.2:n.564+242A>G
XM_006724836.1:c.292+242A>G	XP_006724899.1:n.292+242A>G
XM_006724837.1:c.292+242A>G	XP_006724900.1:n.292+242A>G
XM_006724839.1:c.292+242A>G	XP_006724902.1:n.292+242A>G
XM_006724841.2:c.-57+242A>G	XP_006724904.1:n.-57+242A>G
XM_006724842.2:c.-57+242A>G	XP_006724905.1:n.-57+242A>G
XM_011531189.1:c.292+242A>G	XP_011529491.1:n.292+242A>G
XM_011531190.1:c.-575A>G	XP_011529492.1:n.-575A>G
XM_011531191.1:c.-557A>G	XP_011529493.1:n.-557A>G
XM_011531192.1:c.-678A>G	XP_011529494.1:n.-678A>G
XR_938511.1:n.595+242A>G
XM_006724841.4:c.-57+242A>G	XP_006724904.1:n.-57+242A>G
XM_006724842.4:c.-57+242A>G	XP_006724905.1:n.-57+242A>G
XM_011531191.2:c.-557A>G	XP_011529493.1:n.-557A>G
XM_017029761.1:c.238+242A>G	XP_016885250.1:n.238+242A>G
XM_017029762.1:c.292+242A>G	XP_016885251.1:n.292+242A>G
XM_017029763.1:c.238+242A>G	XP_016885252.1:n.238+242A>G
XM_017029765.2:c.-57+242A>G	XP_016885254.1:n.-57+242A>G
XM_024452431.1:c.292+242A>G	XP_024308199.1:n.292+242A>G
NM_000116.5:c.238+242A>G MANE Select	NP_000107.1:n.238+242A>G
NM_001303465.2:c.292+242A>G	NP_001290394.1:n.292+242A>G
NM_181311.4:c.238+242A>G	NP_851828.1:n.238+242A>G
NM_181312.4:c.238+242A>G	NP_851829.1:n.238+242A>G
NM_181313.4:c.238+242A>G	NP_851830.1:n.238+242A>G
NR_024048.3:n.543+242A>G