Canonical Allele Identifier: CA415185512

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153649066A>T (hg19) ; chrX:g.154420727A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420727A>T , CM000685.2:g.154420727A>T	GRCh38
NC_000023.10:g.153649066A>T , CM000685.1:g.153649066A>T	GRCh37
NC_000023.9:g.153302260A>T	NCBI36
NG_009634.1:g.14190A>T
NG_009634.2:g.14193A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1579A>T
ENST00000698317.1:n.2195A>T
ENST00000698318.1:n.1978A>T
ENST00000698319.1:n.1341A>T
ENST00000698320.1:n.1229A>T
ENST00000470127.2:n.1242A>T
ENST00000475699.6:c.733A>T	ENSP00000419854.3:p.Lys245Ter
ENST00000483674.3:n.651A>T
ENST00000601016.6:c.769A>T MANE Select	ENSP00000469981.1:p.Lys257Ter
ENST00000612012.5:c.727A>T	ENSP00000482070.2:p.Lys243Ter
ENST00000612460.5:c.679A>T	ENSP00000481037.1:p.Lys227Ter
ENST00000614595.2:n.2116A>T
ENST00000615658.5:n.1358A>T
ENST00000616020.5:c.781A>T	ENSP00000483636.2:p.Lys261Ter
ENST00000617701.5:c.*782A>T	ENSP00000481645.1:n.*782A>T
ENST00000651139.1:c.-15A>T	ENSP00000498957.1:n.-15A>T
ENST00000652354.1:c.451A>T	ENSP00000498734.1:p.Lys151Ter
ENST00000652358.1:c.562A>T	ENSP00000498464.1:p.Lys188Ter
ENST00000652390.1:c.688A>T	ENSP00000498858.1:p.Lys230Ter
ENST00000652476.1:n.1435A>T
ENST00000652644.1:c.382A>T	ENSP00000498496.1:p.Lys128Ter
ENST00000652682.1:c.826A>T	ENSP00000498288.1:p.Lys276Ter
ENST00000652685.1:n.1122A>T
ENST00000369776.8:c.679A>T	ENSP00000358791.4:p.Lys227Ter
ENST00000426231.5:c.766A>T
ENST00000475699.5:c.727A>T	ENSP00000419854.2:p.Lys243Ter
ENST00000494912.5:n.1458A>T
ENST00000498029.1:n.227A>T
ENST00000601016.5:c.769A>T	ENSP00000469981.1:p.Lys257Ter
ENST00000612460.4:c.679A>T	ENSP00000481037.1:p.Lys227Ter
ENST00000613002.4:c.637A>T	ENSP00000478154.1:p.Lys213Ter
ENST00000615986.4:c.*497A>T	ENSP00000480133.1:n.*497A>T
NM_000116.4:c.769A>T	NP_000107.1:p.Lys257Ter
NM_001303465.1:c.781A>T	NP_001290394.1:p.Lys261Ter
NM_181311.3:c.679A>T	NP_851828.1:p.Lys227Ter
NM_181312.3:c.727A>T	NP_851829.1:p.Lys243Ter
NM_181313.3:c.637A>T	NP_851830.1:p.Lys213Ter
NR_024048.2:n.1111A>T
XM_006724836.1:c.823A>T	XP_006724899.1:p.Lys275Ter
XM_006724837.1:c.808A>T	XP_006724900.1:p.Lys270Ter
XM_006724839.1:c.691A>T	XP_006724902.1:p.Lys231Ter
XM_006724841.2:c.562A>T	XP_006724904.1:p.Lys188Ter
XM_006724842.2:c.472A>T	XP_006724905.1:p.Lys158Ter
XM_011531189.1:c.610A>T	XP_011529491.1:p.Lys204Ter
XM_011531190.1:c.562A>T	XP_011529492.1:p.Lys188Ter
XM_011531191.1:c.493A>T	XP_011529493.1:p.Lys165Ter
XM_011531192.1:c.490A>T	XP_011529494.1:p.Lys164Ter
XR_938511.1:n.1117A>T
XM_006724841.4:c.562A>T	XP_006724904.1:p.Lys188Ter
XM_006724842.4:c.472A>T	XP_006724905.1:p.Lys158Ter
XM_011531191.2:c.493A>T	XP_011529493.1:p.Lys165Ter
XM_017029761.1:c.754A>T	XP_016885250.1:p.Lys252Ter
XM_017029762.1:c.733A>T	XP_016885251.1:p.Lys245Ter
XM_017029763.1:c.556A>T	XP_016885252.1:p.Lys186Ter
XM_017029764.1:c.490A>T	XP_016885253.1:p.Lys164Ter
XM_017029765.2:c.430A>T	XP_016885254.1:p.Lys144Ter
XM_024452431.1:c.727A>T	XP_024308199.1:p.Lys243Ter
NM_000116.5:c.769A>T MANE Select	NP_000107.1:p.Lys257Ter
NM_001303465.2:c.781A>T	NP_001290394.1:p.Lys261Ter
NM_181311.4:c.679A>T	NP_851828.1:p.Lys227Ter
NM_181312.4:c.727A>T	NP_851829.1:p.Lys243Ter
NM_181313.4:c.637A>T	NP_851830.1:p.Lys213Ter
NR_024048.3:n.1090A>T