Canonical Allele Identifier: CA2466677802

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420721G= , CM000685.2:g.154420721G=	GRCh38
NC_000023.10:g.153649060G= , CM000685.1:g.153649060G=	GRCh37
NC_000023.9:g.153302254G=	NCBI36
NG_009634.1:g.14184G=
NG_009634.2:g.14187G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1573G=
ENST00000698317.1:n.2189G=
ENST00000698318.1:n.1972G=
ENST00000698319.1:n.1335G=
ENST00000698320.1:n.1223G=
ENST00000470127.2:n.1236G=
ENST00000475699.6:c.727G=	ENSP00000419854.3:p.Glu243=
ENST00000483674.3:n.645G=
ENST00000601016.6:c.763G= MANE Select	ENSP00000469981.1:p.Glu255=
ENST00000612012.5:c.721G=	ENSP00000482070.2:p.Glu241=
ENST00000612460.5:c.673G=	ENSP00000481037.1:p.Glu225=
ENST00000614595.2:n.2110G=
ENST00000615658.5:n.1352G=
ENST00000616020.5:c.775G=	ENSP00000483636.2:p.Glu259=
ENST00000617701.5:c.*776G=	ENSP00000481645.1:n.*776G=
ENST00000651139.1:c.-21G=	ENSP00000498957.1:n.-21G=
ENST00000652354.1:c.445G=	ENSP00000498734.1:p.Glu149=
ENST00000652358.1:c.556G=	ENSP00000498464.1:p.Glu186=
ENST00000652390.1:c.682G=	ENSP00000498858.1:p.Glu228=
ENST00000652476.1:n.1429G=
ENST00000652644.1:c.376G=	ENSP00000498496.1:p.Glu126=
ENST00000652682.1:c.820G=	ENSP00000498288.1:p.Glu274=
ENST00000652685.1:n.1116G=
ENST00000369776.8:c.673G=	ENSP00000358791.4:p.Glu225=
ENST00000426231.5:c.760G=
ENST00000475699.5:c.721G=	ENSP00000419854.2:p.Glu241=
ENST00000494912.5:n.1452G=
ENST00000498029.1:n.221G=
ENST00000601016.5:c.763G=	ENSP00000469981.1:p.Glu255=
ENST00000612460.4:c.673G=	ENSP00000481037.1:p.Glu225=
ENST00000613002.4:c.631G=	ENSP00000478154.1:p.Glu211=
ENST00000615986.4:c.*491G=	ENSP00000480133.1:n.*491G=
NM_000116.4:c.763G=	NP_000107.1:p.Glu255=
NM_001303465.1:c.775G=	NP_001290394.1:p.Glu259=
NM_181311.3:c.673G=	NP_851828.1:p.Glu225=
NM_181312.3:c.721G=	NP_851829.1:p.Glu241=
NM_181313.3:c.631G=	NP_851830.1:p.Glu211=
NR_024048.2:n.1105G=
XM_006724836.1:c.817G=	XP_006724899.1:p.Glu273=
XM_006724837.1:c.802G=	XP_006724900.1:p.Glu268=
XM_006724839.1:c.685G=	XP_006724902.1:p.Glu229=
XM_006724841.2:c.556G=	XP_006724904.1:p.Glu186=
XM_006724842.2:c.466G=	XP_006724905.1:p.Glu156=
XM_011531189.1:c.604G=	XP_011529491.1:p.Glu202=
XM_011531190.1:c.556G=	XP_011529492.1:p.Glu186=
XM_011531191.1:c.487G=	XP_011529493.1:p.Glu163=
XM_011531192.1:c.484G=	XP_011529494.1:p.Glu162=
XR_938511.1:n.1111G=
XM_006724841.4:c.556G=	XP_006724904.1:p.Glu186=
XM_006724842.4:c.466G=	XP_006724905.1:p.Glu156=
XM_011531191.2:c.487G=	XP_011529493.1:p.Glu163=
XM_017029761.1:c.748G=	XP_016885250.1:p.Glu250=
XM_017029762.1:c.727G=	XP_016885251.1:p.Glu243=
XM_017029763.1:c.550G=	XP_016885252.1:p.Glu184=
XM_017029764.1:c.484G=	XP_016885253.1:p.Glu162=
XM_017029765.2:c.424G=	XP_016885254.1:p.Glu142=
XM_024452431.1:c.721G=	XP_024308199.1:p.Glu241=
NM_000116.5:c.763G= MANE Select	NP_000107.1:p.Glu255=
NM_001303465.2:c.775G=	NP_001290394.1:p.Glu259=
NM_181311.4:c.673G=	NP_851828.1:p.Glu225=
NM_181312.4:c.721G=	NP_851829.1:p.Glu241=
NM_181313.4:c.631G=	NP_851830.1:p.Glu211=
NR_024048.3:n.1084G=