Canonical Allele Identifier: CA415181906

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153641871T>A (hg19) ; chrX:g.154413534T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413534T>A , CM000685.2:g.154413534T>A	GRCh38
NC_000023.10:g.153641871T>A , CM000685.1:g.153641871T>A	GRCh37
NC_000023.9:g.153295065T>A	NCBI36
NG_009634.1:g.6995T>A
NG_012884.2:g.3555A>T
NG_009634.2:g.7000T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.871T>A
ENST00000698235.1:n.411T>A
ENST00000698317.1:n.1397T>A
ENST00000698318.1:n.1270T>A
ENST00000470127.2:n.615T>A
ENST00000475699.6:c.391T>A	ENSP00000419854.3:p.Phe131Ile
ENST00000476800.2:n.1523T>A
ENST00000483674.3:n.228T>A
ENST00000601016.6:c.337T>A MANE Select	ENSP00000469981.1:p.Phe113Ile
ENST00000612012.5:c.337T>A	ENSP00000482070.2:p.Phe113Ile
ENST00000612460.5:c.337T>A	ENSP00000481037.1:p.Phe113Ile
ENST00000614595.2:n.1774T>A
ENST00000615658.5:n.650T>A
ENST00000616020.5:c.391T>A	ENSP00000483636.2:p.Phe131Ile
ENST00000617701.5:c.*155T>A	ENSP00000481645.1:n.*155T>A
ENST00000621647.2:n.619T>A
ENST00000652354.1:c.61T>A	ENSP00000498734.1:p.Phe21Ile
ENST00000652358.1:c.130T>A	ENSP00000498464.1:p.Phe44Ile
ENST00000652390.1:c.256T>A	ENSP00000498858.1:p.Phe86Ile
ENST00000652476.1:n.727T>A
ENST00000652682.1:c.337T>A	ENSP00000498288.1:p.Phe113Ile
ENST00000652685.1:n.495T>A
ENST00000369776.8:c.262T>A	ENSP00000358791.4:p.Phe88Ile
ENST00000426231.5:c.253T>A
ENST00000439735.2:c.337T>A	ENSP00000398193.1:p.Phe113Ile
ENST00000470127.1:n.6T>A
ENST00000475699.5:c.337T>A	ENSP00000419854.2:p.Phe113Ile
ENST00000476679.5:n.250T>A
ENST00000476800.1:n.444T>A
ENST00000479875.1:n.366T>A
ENST00000483674.2:n.46T>A
ENST00000483780.5:n.111T>A
ENST00000601016.5:c.337T>A	ENSP00000469981.1:p.Phe113Ile
ENST00000612012.4:c.391T>A	ENSP00000482070.1:p.Phe131Ile
ENST00000612460.4:c.337T>A	ENSP00000481037.1:p.Phe113Ile
ENST00000613002.4:c.337T>A	ENSP00000478154.1:p.Phe113Ile
ENST00000613634.4:n.657T>A
ENST00000615658.4:n.750T>A
ENST00000615986.4:c.*155T>A	ENSP00000480133.1:n.*155T>A
ENST00000616020.4:c.391T>A	ENSP00000483636.1:p.Phe131Ile
ENST00000617701.4:c.*167T>A	ENSP00000481645.1:n.*167T>A
ENST00000620808.4:c.*136T>A	ENSP00000479311.1:n.*136T>A
ENST00000621647.1:n.851T>A
NM_000116.4:c.337T>A	NP_000107.1:p.Phe113Ile
NM_001303465.1:c.391T>A	NP_001290394.1:p.Phe131Ile
NM_181311.3:c.337T>A	NP_851828.1:p.Phe113Ile
NM_181312.3:c.337T>A	NP_851829.1:p.Phe113Ile
NM_181313.3:c.337T>A	NP_851830.1:p.Phe113Ile
NR_024048.2:n.769T>A
XM_006724836.1:c.391T>A	XP_006724899.1:p.Phe131Ile
XM_006724837.1:c.391T>A	XP_006724900.1:p.Phe131Ile
XM_006724839.1:c.391T>A	XP_006724902.1:p.Phe131Ile
XM_006724841.2:c.130T>A	XP_006724904.1:p.Phe44Ile
XM_006724842.2:c.130T>A	XP_006724905.1:p.Phe44Ile
XM_011531189.1:c.391T>A	XP_011529491.1:p.Phe131Ile
XM_011531190.1:c.130T>A	XP_011529492.1:p.Phe44Ile
XM_011531191.1:c.61T>A	XP_011529493.1:p.Phe21Ile
XM_011531192.1:c.58T>A	XP_011529494.1:p.Phe20Ile
XR_938511.1:n.694T>A
XM_006724841.4:c.130T>A	XP_006724904.1:p.Phe44Ile
XM_006724842.4:c.130T>A	XP_006724905.1:p.Phe44Ile
XM_011531191.2:c.61T>A	XP_011529493.1:p.Phe21Ile
XM_017029761.1:c.337T>A	XP_016885250.1:p.Phe113Ile
XM_017029762.1:c.391T>A	XP_016885251.1:p.Phe131Ile
XM_017029763.1:c.337T>A	XP_016885252.1:p.Phe113Ile
XM_017029764.1:c.58T>A	XP_016885253.1:p.Phe20Ile
XM_017029765.2:c.130T>A	XP_016885254.1:p.Phe44Ile
XM_024452431.1:c.391T>A	XP_024308199.1:p.Phe131Ile
NM_000116.5:c.337T>A MANE Select	NP_000107.1:p.Phe113Ile
NM_001303465.2:c.391T>A	NP_001290394.1:p.Phe131Ile
NM_181311.4:c.337T>A	NP_851828.1:p.Phe113Ile
NM_181312.4:c.337T>A	NP_851829.1:p.Phe113Ile
NM_181313.4:c.337T>A	NP_851830.1:p.Phe113Ile
NR_024048.3:n.748T>A