Canonical Allele Identifier: CA2466675362

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413544G= , CM000685.2:g.154413544G=	GRCh38
NC_000023.10:g.153641881G= , CM000685.1:g.153641881G=	GRCh37
NC_000023.9:g.153295075G=	NCBI36
NG_009634.1:g.7005G=
NG_012884.2:g.3545C=
NG_009634.2:g.7010G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.881G=
ENST00000698235.1:n.421G=
ENST00000698317.1:n.1407G=
ENST00000698318.1:n.1280G=
ENST00000470127.2:n.625G=
ENST00000475699.6:c.401G=	ENSP00000419854.3:p.Gly134=
ENST00000476800.2:n.1533G=
ENST00000483674.3:n.238G=
ENST00000601016.6:c.347G= MANE Select	ENSP00000469981.1:p.Gly116=
ENST00000612012.5:c.347G=	ENSP00000482070.2:p.Gly116=
ENST00000612460.5:c.347G=	ENSP00000481037.1:p.Gly116=
ENST00000614595.2:n.1784G=
ENST00000615658.5:n.660G=
ENST00000616020.5:c.401G=	ENSP00000483636.2:p.Gly134=
ENST00000617701.5:c.*165G=	ENSP00000481645.1:n.*165G=
ENST00000621647.2:n.629G=
ENST00000652354.1:c.71G=	ENSP00000498734.1:p.Gly24=
ENST00000652358.1:c.140G=	ENSP00000498464.1:p.Gly47=
ENST00000652390.1:c.266G=	ENSP00000498858.1:p.Gly89=
ENST00000652476.1:n.737G=
ENST00000652682.1:c.347G=	ENSP00000498288.1:p.Gly116=
ENST00000652685.1:n.505G=
ENST00000369776.8:c.272G=	ENSP00000358791.4:p.Gly91=
ENST00000426231.5:c.263G=
ENST00000439735.2:c.347G=	ENSP00000398193.1:p.Gly116=
ENST00000470127.1:n.16G=
ENST00000475699.5:c.347G=	ENSP00000419854.2:p.Gly116=
ENST00000476679.5:n.260G=
ENST00000476800.1:n.454G=
ENST00000479875.1:n.376G=
ENST00000483674.2:n.56G=
ENST00000483780.5:n.121G=
ENST00000601016.5:c.347G=	ENSP00000469981.1:p.Gly116=
ENST00000612012.4:c.401G=	ENSP00000482070.1:p.Gly134=
ENST00000612460.4:c.347G=	ENSP00000481037.1:p.Gly116=
ENST00000613002.4:c.347G=	ENSP00000478154.1:p.Gly116=
ENST00000613634.4:n.667G=
ENST00000615658.4:n.760G=
ENST00000615986.4:c.*165G=	ENSP00000480133.1:n.*165G=
ENST00000616020.4:c.401G=	ENSP00000483636.1:p.Gly134=
ENST00000617701.4:c.*177G=	ENSP00000481645.1:n.*177G=
ENST00000620808.4:c.*146G=	ENSP00000479311.1:n.*146G=
ENST00000621647.1:n.861G=
NM_000116.4:c.347G=	NP_000107.1:p.Gly116=
NM_001303465.1:c.401G=	NP_001290394.1:p.Gly134=
NM_181311.3:c.347G=	NP_851828.1:p.Gly116=
NM_181312.3:c.347G=	NP_851829.1:p.Gly116=
NM_181313.3:c.347G=	NP_851830.1:p.Gly116=
NR_024048.2:n.779G=
XM_006724836.1:c.401G=	XP_006724899.1:p.Gly134=
XM_006724837.1:c.401G=	XP_006724900.1:p.Gly134=
XM_006724839.1:c.401G=	XP_006724902.1:p.Gly134=
XM_006724841.2:c.140G=	XP_006724904.1:p.Gly47=
XM_006724842.2:c.140G=	XP_006724905.1:p.Gly47=
XM_011531189.1:c.401G=	XP_011529491.1:p.Gly134=
XM_011531190.1:c.140G=	XP_011529492.1:p.Gly47=
XM_011531191.1:c.71G=	XP_011529493.1:p.Gly24=
XM_011531192.1:c.68G=	XP_011529494.1:p.Gly23=
XR_938511.1:n.704G=
XM_006724841.4:c.140G=	XP_006724904.1:p.Gly47=
XM_006724842.4:c.140G=	XP_006724905.1:p.Gly47=
XM_011531191.2:c.71G=	XP_011529493.1:p.Gly24=
XM_017029761.1:c.347G=	XP_016885250.1:p.Gly116=
XM_017029762.1:c.401G=	XP_016885251.1:p.Gly134=
XM_017029763.1:c.347G=	XP_016885252.1:p.Gly116=
XM_017029764.1:c.68G=	XP_016885253.1:p.Gly23=
XM_017029765.2:c.140G=	XP_016885254.1:p.Gly47=
XM_024452431.1:c.401G=	XP_024308199.1:p.Gly134=
NM_000116.5:c.347G= MANE Select	NP_000107.1:p.Gly116=
NM_001303465.2:c.401G=	NP_001290394.1:p.Gly134=
NM_181311.4:c.347G=	NP_851828.1:p.Gly116=
NM_181312.4:c.347G=	NP_851829.1:p.Gly116=
NM_181313.4:c.347G=	NP_851830.1:p.Gly116=
NR_024048.3:n.758G=