Canonical Allele Identifier: CA2466677622

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420223G= , CM000685.2:g.154420223G=	GRCh38
NC_000023.10:g.153648562G= , CM000685.1:g.153648562G=	GRCh37
NC_000023.9:g.153301756G=	NCBI36
NG_009634.1:g.13686G=
NG_009634.2:g.13689G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.1468G=
ENST00000698317.1:n.2084G=
ENST00000698318.1:n.1867G=
ENST00000698319.1:n.1230G=
ENST00000698320.1:n.1118G=
ENST00000470127.2:n.1131G=
ENST00000475699.6:c.622G=	ENSP00000419854.3:p.Val208=
ENST00000483674.3:n.540G=
ENST00000601016.6:c.658G= MANE Select	ENSP00000469981.1:p.Val220=
ENST00000612012.5:c.616G=	ENSP00000482070.2:p.Val206=
ENST00000612460.5:c.568G=	ENSP00000481037.1:p.Val190=
ENST00000614595.2:n.2005G=
ENST00000615658.5:n.1247G=
ENST00000616020.5:c.670G=	ENSP00000483636.2:p.Val224=
ENST00000617701.5:c.*671G=	ENSP00000481645.1:n.*671G=
ENST00000652354.1:c.340G=	ENSP00000498734.1:p.Val114=
ENST00000652358.1:c.451G=	ENSP00000498464.1:p.Val151=
ENST00000652390.1:c.577G=	ENSP00000498858.1:p.Val193=
ENST00000652476.1:n.1324G=
ENST00000652644.1:c.271G=	ENSP00000498496.1:p.Val91=
ENST00000652682.1:c.715G=	ENSP00000498288.1:p.Val239=
ENST00000652685.1:n.1011G=
ENST00000369776.8:c.568G=	ENSP00000358791.4:p.Val190=
ENST00000426231.5:c.655G=
ENST00000475699.5:c.616G=	ENSP00000419854.2:p.Val206=
ENST00000494912.5:n.1347G=
ENST00000498029.1:n.116G=
ENST00000601016.5:c.658G=	ENSP00000469981.1:p.Val220=
ENST00000612460.4:c.568G=	ENSP00000481037.1:p.Val190=
ENST00000613002.4:c.526G=	ENSP00000478154.1:p.Val176=
ENST00000615986.4:c.*386G=	ENSP00000480133.1:n.*386G=
NM_000116.4:c.658G=	NP_000107.1:p.Val220=
NM_001303465.1:c.670G=	NP_001290394.1:p.Val224=
NM_181311.3:c.568G=	NP_851828.1:p.Val190=
NM_181312.3:c.616G=	NP_851829.1:p.Val206=
NM_181313.3:c.526G=	NP_851830.1:p.Val176=
NR_024048.2:n.1000G=
XM_006724836.1:c.712G=	XP_006724899.1:p.Val238=
XM_006724837.1:c.697G=	XP_006724900.1:p.Val233=
XM_006724839.1:c.580G=	XP_006724902.1:p.Val194=
XM_006724841.2:c.451G=	XP_006724904.1:p.Val151=
XM_006724842.2:c.361G=	XP_006724905.1:p.Val121=
XM_011531189.1:c.499G=	XP_011529491.1:p.Val167=
XM_011531190.1:c.451G=	XP_011529492.1:p.Val151=
XM_011531191.1:c.382G=	XP_011529493.1:p.Val128=
XM_011531192.1:c.379G=	XP_011529494.1:p.Val127=
XR_938511.1:n.1006G=
XM_006724841.4:c.451G=	XP_006724904.1:p.Val151=
XM_006724842.4:c.361G=	XP_006724905.1:p.Val121=
XM_011531191.2:c.382G=	XP_011529493.1:p.Val128=
XM_017029761.1:c.643G=	XP_016885250.1:p.Val215=
XM_017029762.1:c.622G=	XP_016885251.1:p.Val208=
XM_017029763.1:c.445G=	XP_016885252.1:p.Val149=
XM_017029764.1:c.379G=	XP_016885253.1:p.Val127=
XM_017029765.2:c.319G=	XP_016885254.1:p.Val107=
XM_024452431.1:c.616G=	XP_024308199.1:p.Val206=
NM_000116.5:c.658G= MANE Select	NP_000107.1:p.Val220=
NM_001303465.2:c.670G=	NP_001290394.1:p.Val224=
NM_181311.4:c.568G=	NP_851828.1:p.Val190=
NM_181312.4:c.616G=	NP_851829.1:p.Val206=
NM_181313.4:c.526G=	NP_851830.1:p.Val176=
NR_024048.3:n.979G=