Canonical Allele Identifier: CA415180288

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153640552G>T (hg19) ; chrX:g.154412215G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154412215G>T , CM000685.2:g.154412215G>T	GRCh38
NC_000023.10:g.153640552G>T , CM000685.1:g.153640552G>T	GRCh37
NC_000023.9:g.153293746G>T	NCBI36
NG_009634.1:g.5676G>T
NG_012884.2:g.4874C>A
NG_009634.2:g.5681G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.666+1G>T
ENST00000698235.1:n.225+1G>T
ENST00000698317.1:n.201G>T
ENST00000698318.1:n.62G>T
ENST00000475699.6:c.292+1G>T	ENSP00000419854.3:n.292+1G>T
ENST00000476800.2:n.204G>T
ENST00000483674.3:n.129+1G>T
ENST00000601016.6:c.238+1G>T MANE Select	ENSP00000469981.1:n.238+1G>T
ENST00000612012.5:c.238+1G>T	ENSP00000482070.2:n.238+1G>T
ENST00000612460.5:c.238+1G>T	ENSP00000481037.1:n.238+1G>T
ENST00000614595.2:n.597G>T
ENST00000615658.5:n.551+1G>T
ENST00000616020.5:c.292+1G>T	ENSP00000483636.2:n.292+1G>T
ENST00000617701.5:c.238+1G>T	ENSP00000481645.1:n.238+1G>T
ENST00000621647.2:n.291+1G>T
ENST00000652358.1:c.-57+263G>T	ENSP00000498464.1:n.-57+263G>T
ENST00000652390.1:c.157+1G>T	ENSP00000498858.1:n.157+1G>T
ENST00000652476.1:n.399+1G>T
ENST00000652682.1:c.238+1G>T	ENSP00000498288.1:n.238+1G>T
ENST00000652685.1:n.290+1G>T
ENST00000369776.8:c.163+209G>T	ENSP00000358791.4:n.163+209G>T
ENST00000426231.5:c.54+1G>T
ENST00000439735.2:c.238+1G>T	ENSP00000398193.1:n.238+1G>T
ENST00000475699.5:c.238+1G>T	ENSP00000419854.2:n.238+1G>T
ENST00000483780.5:n.12+1G>T
ENST00000601016.5:c.238+1G>T	ENSP00000469981.1:n.238+1G>T
ENST00000612012.4:c.292+1G>T	ENSP00000482070.1:n.292+1G>T
ENST00000612460.4:c.238+1G>T	ENSP00000481037.1:n.238+1G>T
ENST00000613002.4:c.238+1G>T	ENSP00000478154.1:n.238+1G>T
ENST00000613634.4:n.558+1G>T
ENST00000614595.1:n.458G>T
ENST00000615658.4:n.564+1G>T
ENST00000615986.4:c.238+1G>T	ENSP00000480133.1:n.238+1G>T
ENST00000616020.4:c.292+1G>T	ENSP00000483636.1:n.292+1G>T
ENST00000617701.4:c.238+1G>T	ENSP00000481645.1:n.238+1G>T
ENST00000620808.4:c.238+1G>T	ENSP00000479311.1:n.238+1G>T
ENST00000621647.1:n.523+1G>T
NM_000116.4:c.238+1G>T	NP_000107.1:n.238+1G>T
NM_001303465.1:c.292+1G>T	NP_001290394.1:n.292+1G>T
NM_181311.3:c.238+1G>T	NP_851828.1:n.238+1G>T
NM_181312.3:c.238+1G>T	NP_851829.1:n.238+1G>T
NM_181313.3:c.238+1G>T	NP_851830.1:n.238+1G>T
NR_024048.2:n.564+1G>T
XM_006724836.1:c.292+1G>T	XP_006724899.1:n.292+1G>T
XM_006724837.1:c.292+1G>T	XP_006724900.1:n.292+1G>T
XM_006724839.1:c.292+1G>T	XP_006724902.1:n.292+1G>T
XM_006724841.2:c.-57+1G>T	XP_006724904.1:n.-57+1G>T
XM_006724842.2:c.-57+1G>T	XP_006724905.1:n.-57+1G>T
XM_011531189.1:c.292+1G>T	XP_011529491.1:n.292+1G>T
XR_938511.1:n.595+1G>T
XM_006724841.4:c.-57+1G>T	XP_006724904.1:n.-57+1G>T
XM_006724842.4:c.-57+1G>T	XP_006724905.1:n.-57+1G>T
XM_017029761.1:c.238+1G>T	XP_016885250.1:n.238+1G>T
XM_017029762.1:c.292+1G>T	XP_016885251.1:n.292+1G>T
XM_017029763.1:c.238+1G>T	XP_016885252.1:n.238+1G>T
XM_017029765.2:c.-57+1G>T	XP_016885254.1:n.-57+1G>T
XM_024452431.1:c.292+1G>T	XP_024308199.1:n.292+1G>T
NM_000116.5:c.238+1G>T MANE Select	NP_000107.1:n.238+1G>T
NM_001303465.2:c.292+1G>T	NP_001290394.1:n.292+1G>T
NM_181311.4:c.238+1G>T	NP_851828.1:n.238+1G>T
NM_181312.4:c.238+1G>T	NP_851829.1:n.238+1G>T
NM_181313.4:c.238+1G>T	NP_851830.1:n.238+1G>T
NR_024048.3:n.543+1G>T