Canonical Allele Identifier: CA415183978

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153648079A>T (hg19) ; chrX:g.154419740A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154419740A>T , CM000685.2:g.154419740A>T	GRCh38
NC_000023.10:g.153648079A>T , CM000685.1:g.153648079A>T	GRCh37
NC_000023.9:g.153301273A>T	NCBI36
NG_009634.1:g.13203A>T
NG_009634.2:g.13206A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1102A>T
ENST00000698317.1:n.1718A>T
ENST00000698318.1:n.1501A>T
ENST00000698319.1:n.864A>T
ENST00000698320.1:n.752A>T
ENST00000470127.2:n.765A>T
ENST00000475699.6:c.541A>T	ENSP00000419854.3:p.Lys181Ter
ENST00000483674.3:n.459A>T
ENST00000601016.6:c.577A>T MANE Select	ENSP00000469981.1:p.Lys193Ter
ENST00000612012.5:c.541+117A>T	ENSP00000482070.2:n.541+117A>T
ENST00000612460.5:c.487A>T	ENSP00000481037.1:p.Lys163Ter
ENST00000614595.2:n.1924A>T
ENST00000615658.5:n.881A>T
ENST00000616020.5:c.595+117A>T	ENSP00000483636.2:n.595+117A>T
ENST00000617701.5:c.*305A>T	ENSP00000481645.1:n.*305A>T
ENST00000652354.1:c.265+117A>T	ENSP00000498734.1:n.265+117A>T
ENST00000652358.1:c.370A>T	ENSP00000498464.1:p.Lys124Ter
ENST00000652390.1:c.496A>T	ENSP00000498858.1:p.Lys166Ter
ENST00000652476.1:n.958A>T
ENST00000652644.1:c.190A>T	ENSP00000498496.1:p.Lys64Ter
ENST00000652682.1:c.634A>T	ENSP00000498288.1:p.Lys212Ter
ENST00000652685.1:n.645A>T
ENST00000369776.8:c.376+117A>T	ENSP00000358791.4:n.376+117A>T
ENST00000426231.5:c.574A>T
ENST00000439735.2:c.484A>T	ENSP00000398193.1:p.Lys162Ter
ENST00000470127.1:n.156A>T
ENST00000475699.5:c.541+117A>T	ENSP00000419854.2:n.541+117A>T
ENST00000476679.5:n.571A>T
ENST00000483780.5:n.342A>T
ENST00000494912.5:n.1266A>T
ENST00000601016.5:c.577A>T	ENSP00000469981.1:p.Lys193Ter
ENST00000612012.4:c.541A>T	ENSP00000482070.1:p.Lys181Ter
ENST00000612460.4:c.487A>T	ENSP00000481037.1:p.Lys163Ter
ENST00000613002.4:c.451+117A>T	ENSP00000478154.1:n.451+117A>T
ENST00000613634.4:n.807A>T
ENST00000615658.4:n.981A>T
ENST00000615986.4:c.*305A>T	ENSP00000480133.1:n.*305A>T
ENST00000620808.4:c.*170-292A>T	ENSP00000479311.1:n.*170-292A>T
NM_000116.4:c.577A>T	NP_000107.1:p.Lys193Ter
NM_001303465.1:c.595+117A>T	NP_001290394.1:n.595+117A>T
NM_181311.3:c.487A>T	NP_851828.1:p.Lys163Ter
NM_181312.3:c.541+117A>T	NP_851829.1:n.541+117A>T
NM_181313.3:c.451+117A>T	NP_851830.1:n.451+117A>T
NR_024048.2:n.919A>T
XM_006724836.1:c.631A>T	XP_006724899.1:p.Lys211Ter
XM_006724837.1:c.505+117A>T	XP_006724900.1:n.505+117A>T
XM_006724839.1:c.505+117A>T	XP_006724902.1:n.505+117A>T
XM_006724841.2:c.370A>T	XP_006724904.1:p.Lys124Ter
XM_006724842.2:c.280A>T	XP_006724905.1:p.Lys94Ter
XM_011531189.1:c.425-292A>T	XP_011529491.1:n.425-292A>T
XM_011531190.1:c.370A>T	XP_011529492.1:p.Lys124Ter
XM_011531191.1:c.301A>T	XP_011529493.1:p.Lys101Ter
XM_011531192.1:c.298A>T	XP_011529494.1:p.Lys100Ter
XR_938511.1:n.925A>T
XM_006724841.4:c.370A>T	XP_006724904.1:p.Lys124Ter
XM_006724842.4:c.280A>T	XP_006724905.1:p.Lys94Ter
XM_011531191.2:c.301A>T	XP_011529493.1:p.Lys101Ter
XM_017029761.1:c.451+117A>T	XP_016885250.1:n.451+117A>T
XM_017029762.1:c.541A>T	XP_016885251.1:p.Lys181Ter
XM_017029763.1:c.371-292A>T	XP_016885252.1:n.371-292A>T
XM_017029764.1:c.298A>T	XP_016885253.1:p.Lys100Ter
XM_017029765.2:c.244+117A>T	XP_016885254.1:n.244+117A>T
XM_024452431.1:c.425-292A>T	XP_024308199.1:n.425-292A>T
NM_000116.5:c.577A>T MANE Select	NP_000107.1:p.Lys193Ter
NM_001303465.2:c.595+117A>T	NP_001290394.1:n.595+117A>T
NM_181311.4:c.487A>T	NP_851828.1:p.Lys163Ter
NM_181312.4:c.541+117A>T	NP_851829.1:n.541+117A>T
NM_181313.4:c.451+117A>T	NP_851830.1:n.451+117A>T
NR_024048.3:n.898A>T