Canonical Allele Identifier: CA2546846396

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154419835T>G , CM000685.2:g.154419835T>G	GRCh38
NC_000023.10:g.153648174T>G , CM000685.1:g.153648174T>G	GRCh37
NC_000023.9:g.153301368T>G	NCBI36
NG_009634.1:g.13298T>G
NG_009634.2:g.13301T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1197T>G
ENST00000698317.1:n.1813T>G
ENST00000698318.1:n.1596T>G
ENST00000698319.1:n.959T>G
ENST00000698320.1:n.847T>G
ENST00000470127.2:n.860T>G
ENST00000475699.6:c.547+89T>G	ENSP00000419854.3:n.547+89T>G
ENST00000483674.3:n.465+89T>G
ENST00000601016.6:c.583+89T>G MANE Select	ENSP00000469981.1:n.583+89T>G
ENST00000612012.5:c.542-197T>G	ENSP00000482070.2:n.542-197T>G
ENST00000612460.5:c.493+89T>G	ENSP00000481037.1:n.493+89T>G
ENST00000614595.2:n.1930+89T>G
ENST00000615658.5:n.976T>G
ENST00000616020.5:c.596-197T>G	ENSP00000483636.2:n.596-197T>G
ENST00000617701.5:c.*400T>G	ENSP00000481645.1:n.*400T>G
ENST00000652354.1:c.266-197T>G	ENSP00000498734.1:n.266-197T>G
ENST00000652358.1:c.376+89T>G	ENSP00000498464.1:n.376+89T>G
ENST00000652390.1:c.502+89T>G	ENSP00000498858.1:n.502+89T>G
ENST00000652476.1:n.1053T>G
ENST00000652644.1:c.196+89T>G	ENSP00000498496.1:n.196+89T>G
ENST00000652682.1:c.640+89T>G	ENSP00000498288.1:n.640+89T>G
ENST00000652685.1:n.740T>G
ENST00000369776.8:c.377-197T>G	ENSP00000358791.4:n.377-197T>G
ENST00000426231.5:c.580+89T>G
ENST00000439735.2:c.490+89T>G	ENSP00000398193.1:n.490+89T>G
ENST00000470127.1:n.162+89T>G
ENST00000475699.5:c.542-197T>G	ENSP00000419854.2:n.542-197T>G
ENST00000476679.5:n.666T>G
ENST00000494912.5:n.1272+89T>G
ENST00000601016.5:c.583+89T>G	ENSP00000469981.1:n.583+89T>G
ENST00000612012.4:c.547+89T>G	ENSP00000482070.1:n.547+89T>G
ENST00000612460.4:c.493+89T>G	ENSP00000481037.1:n.493+89T>G
ENST00000613002.4:c.452-197T>G	ENSP00000478154.1:n.452-197T>G
ENST00000613634.4:n.902T>G
ENST00000615658.4:n.1076T>G
ENST00000615986.4:c.*311+89T>G	ENSP00000480133.1:n.*311+89T>G
ENST00000620808.4:c.*170-197T>G	ENSP00000479311.1:n.*170-197T>G
NM_000116.4:c.583+89T>G	NP_000107.1:n.583+89T>G
NM_001303465.1:c.596-197T>G	NP_001290394.1:n.596-197T>G
NM_181311.3:c.493+89T>G	NP_851828.1:n.493+89T>G
NM_181312.3:c.542-197T>G	NP_851829.1:n.542-197T>G
NM_181313.3:c.452-197T>G	NP_851830.1:n.452-197T>G
NR_024048.2:n.925+89T>G
XM_006724836.1:c.637+89T>G	XP_006724899.1:n.637+89T>G
XM_006724837.1:c.506-197T>G	XP_006724900.1:n.506-197T>G
XM_006724839.1:c.506-197T>G	XP_006724902.1:n.506-197T>G
XM_006724841.2:c.376+89T>G	XP_006724904.1:n.376+89T>G
XM_006724842.2:c.286+89T>G	XP_006724905.1:n.286+89T>G
XM_011531189.1:c.425-197T>G	XP_011529491.1:n.425-197T>G
XM_011531190.1:c.376+89T>G	XP_011529492.1:n.376+89T>G
XM_011531191.1:c.307+89T>G	XP_011529493.1:n.307+89T>G
XM_011531192.1:c.304+89T>G	XP_011529494.1:n.304+89T>G
XR_938511.1:n.931+89T>G
XM_006724841.4:c.376+89T>G	XP_006724904.1:n.376+89T>G
XM_006724842.4:c.286+89T>G	XP_006724905.1:n.286+89T>G
XM_011531191.2:c.307+89T>G	XP_011529493.1:n.307+89T>G
XM_017029761.1:c.452-197T>G	XP_016885250.1:n.452-197T>G
XM_017029762.1:c.547+89T>G	XP_016885251.1:n.547+89T>G
XM_017029763.1:c.371-197T>G	XP_016885252.1:n.371-197T>G
XM_017029764.1:c.304+89T>G	XP_016885253.1:n.304+89T>G
XM_017029765.2:c.245-197T>G	XP_016885254.1:n.245-197T>G
XM_024452431.1:c.425-197T>G	XP_024308199.1:n.425-197T>G
NM_000116.5:c.583+89T>G MANE Select	NP_000107.1:n.583+89T>G
NM_001303465.2:c.596-197T>G	NP_001290394.1:n.596-197T>G
NM_181311.4:c.493+89T>G	NP_851828.1:n.493+89T>G
NM_181312.4:c.542-197T>G	NP_851829.1:n.542-197T>G
NM_181313.4:c.452-197T>G	NP_851830.1:n.452-197T>G
NR_024048.3:n.904+89T>G