Canonical Allele Identifier: CA2466675268

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413280G= , CM000685.2:g.154413280G=	GRCh38
NC_000023.10:g.153641617G= , CM000685.1:g.153641617G=	GRCh37
NC_000023.9:g.153294811G=	NCBI36
NG_009634.1:g.6741G=
NG_012884.2:g.3809C=
NG_009634.2:g.6746G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.740G=
ENST00000698235.1:n.299G=
ENST00000698317.1:n.1266G=
ENST00000698318.1:n.1127G=
ENST00000470127.2:n.361G=
ENST00000475699.6:c.338+28G=	ENSP00000419854.3:n.338+28G=
ENST00000476800.2:n.1269G=
ENST00000483674.3:n.175+28G=
ENST00000601016.6:c.284+28G= MANE Select	ENSP00000469981.1:n.284+28G=
ENST00000612012.5:c.284+28G=	ENSP00000482070.2:n.284+28G=
ENST00000612460.5:c.284+28G=	ENSP00000481037.1:n.284+28G=
ENST00000614595.2:n.1662G=
ENST00000615658.5:n.597+28G=
ENST00000616020.5:c.338+28G=	ENSP00000483636.2:n.338+28G=
ENST00000617701.5:c.*24G=	ENSP00000481645.1:n.*24G=
ENST00000621647.2:n.365G=
ENST00000652354.1:c.8+28G=	ENSP00000498734.1:n.8+28G=
ENST00000652358.1:c.18G=	ENSP00000498464.1:p.Trp6=
ENST00000652390.1:c.203+28G=	ENSP00000498858.1:n.203+28G=
ENST00000652476.1:n.473G=
ENST00000652682.1:c.284+28G=	ENSP00000498288.1:n.284+28G=
ENST00000652685.1:n.364G=
ENST00000369776.8:c.209+28G=	ENSP00000358791.4:n.209+28G=
ENST00000426231.5:c.128G=
ENST00000439735.2:c.284+28G=	ENSP00000398193.1:n.284+28G=
ENST00000475699.5:c.284+28G=	ENSP00000419854.2:n.284+28G=
ENST00000476679.5:n.197+28G=
ENST00000476800.1:n.190G=
ENST00000479875.1:n.313+28G=
ENST00000483780.5:n.58+28G=
ENST00000601016.5:c.284+28G=	ENSP00000469981.1:n.284+28G=
ENST00000612012.4:c.338+28G=	ENSP00000482070.1:n.338+28G=
ENST00000612460.4:c.284+28G=	ENSP00000481037.1:n.284+28G=
ENST00000613002.4:c.284+28G=	ENSP00000478154.1:n.284+28G=
ENST00000613634.4:n.604+28G=
ENST00000615658.4:n.638G=
ENST00000615986.4:c.*24G=	ENSP00000480133.1:n.*24G=
ENST00000616020.4:c.338+28G=	ENSP00000483636.1:n.338+28G=
ENST00000617701.4:c.*24G=	ENSP00000481645.1:n.*24G=
ENST00000620808.4:c.*24G=	ENSP00000479311.1:n.*24G=
ENST00000621647.1:n.597G=
NM_000116.4:c.284+28G=	NP_000107.1:n.284+28G=
NM_001303465.1:c.338+28G=	NP_001290394.1:n.338+28G=
NM_181311.3:c.284+28G=	NP_851828.1:n.284+28G=
NM_181312.3:c.284+28G=	NP_851829.1:n.284+28G=
NM_181313.3:c.284+28G=	NP_851830.1:n.284+28G=
NR_024048.2:n.638G=
XM_006724836.1:c.338+28G=	XP_006724899.1:n.338+28G=
XM_006724837.1:c.338+28G=	XP_006724900.1:n.338+28G=
XM_006724839.1:c.338+28G=	XP_006724902.1:n.338+28G=
XM_006724841.2:c.18G=	XP_006724904.1:p.Trp6=
XM_006724842.2:c.18G=	XP_006724905.1:p.Trp6=
XM_011531189.1:c.338+28G=	XP_011529491.1:n.338+28G=
XM_011531190.1:c.18G=	XP_011529492.1:p.Trp6=
XM_011531191.1:c.8+28G=	XP_011529493.1:n.8+28G=
XM_011531192.1:c.-86G=	XP_011529494.1:n.-86G=
XR_938511.1:n.641+28G=
XM_006724841.4:c.18G=	XP_006724904.1:p.Trp6=
XM_006724842.4:c.18G=	XP_006724905.1:p.Trp6=
XM_011531191.2:c.8+28G=	XP_011529493.1:n.8+28G=
XM_017029761.1:c.284+28G=	XP_016885250.1:n.284+28G=
XM_017029762.1:c.338+28G=	XP_016885251.1:n.338+28G=
XM_017029763.1:c.284+28G=	XP_016885252.1:n.284+28G=
XM_017029764.1:c.-86G=	XP_016885253.1:n.-86G=
XM_017029765.2:c.18G=	XP_016885254.1:p.Trp6=
XM_024452431.1:c.338+28G=	XP_024308199.1:n.338+28G=
NM_000116.5:c.284+28G= MANE Select	NP_000107.1:n.284+28G=
NM_001303465.2:c.338+28G=	NP_001290394.1:n.338+28G=
NM_181311.4:c.284+28G=	NP_851828.1:n.284+28G=
NM_181312.4:c.284+28G=	NP_851829.1:n.284+28G=
NM_181313.4:c.284+28G=	NP_851830.1:n.284+28G=
NR_024048.3:n.617G=