Canonical Allele Identifier: CA2695123659

Gene: TAFAZZIN

Linked Data

• gnomAD v4: X-154419888-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154419888G>T , CM000685.2:g.154419888G>T	GRCh38
NC_000023.10:g.153648227G>T , CM000685.1:g.153648227G>T	GRCh37
NC_000023.9:g.153301421G>T	NCBI36
NG_009634.1:g.13351G>T
NG_009634.2:g.13354G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.1250G>T
ENST00000698317.1:n.1866G>T
ENST00000698318.1:n.1649G>T
ENST00000698319.1:n.1012G>T
ENST00000698320.1:n.900G>T
ENST00000470127.2:n.913G>T
ENST00000475699.6:c.547+142G>T	ENSP00000419854.3:n.547+142G>T
ENST00000483674.3:n.465+142G>T
ENST00000601016.6:c.583+142G>T MANE Select	ENSP00000469981.1:n.583+142G>T
ENST00000612012.5:c.542-144G>T	ENSP00000482070.2:n.542-144G>T
ENST00000612460.5:c.493+142G>T	ENSP00000481037.1:n.493+142G>T
ENST00000614595.2:n.1930+142G>T
ENST00000615658.5:n.1029G>T
ENST00000616020.5:c.596-144G>T	ENSP00000483636.2:n.596-144G>T
ENST00000617701.5:c.*453G>T	ENSP00000481645.1:n.*453G>T
ENST00000652354.1:c.266-144G>T	ENSP00000498734.1:n.266-144G>T
ENST00000652358.1:c.376+142G>T	ENSP00000498464.1:n.376+142G>T
ENST00000652390.1:c.502+142G>T	ENSP00000498858.1:n.502+142G>T
ENST00000652476.1:n.1106G>T
ENST00000652644.1:c.196+142G>T	ENSP00000498496.1:n.196+142G>T
ENST00000652682.1:c.640+142G>T	ENSP00000498288.1:n.640+142G>T
ENST00000652685.1:n.793G>T
ENST00000369776.8:c.377-144G>T	ENSP00000358791.4:n.377-144G>T
ENST00000426231.5:c.580+142G>T
ENST00000439735.2:c.490+142G>T	ENSP00000398193.1:n.490+142G>T
ENST00000470127.1:n.162+142G>T
ENST00000475699.5:c.542-144G>T	ENSP00000419854.2:n.542-144G>T
ENST00000476679.5:n.719G>T
ENST00000494912.5:n.1272+142G>T
ENST00000601016.5:c.583+142G>T	ENSP00000469981.1:n.583+142G>T
ENST00000612012.4:c.547+142G>T	ENSP00000482070.1:n.547+142G>T
ENST00000612460.4:c.493+142G>T	ENSP00000481037.1:n.493+142G>T
ENST00000613002.4:c.452-144G>T	ENSP00000478154.1:n.452-144G>T
ENST00000613634.4:n.955G>T
ENST00000615658.4:n.1129G>T
ENST00000615986.4:c.*311+142G>T	ENSP00000480133.1:n.*311+142G>T
ENST00000620808.4:c.*170-144G>T	ENSP00000479311.1:n.*170-144G>T
NM_000116.4:c.583+142G>T	NP_000107.1:n.583+142G>T
NM_001303465.1:c.596-144G>T	NP_001290394.1:n.596-144G>T
NM_181311.3:c.493+142G>T	NP_851828.1:n.493+142G>T
NM_181312.3:c.542-144G>T	NP_851829.1:n.542-144G>T
NM_181313.3:c.452-144G>T	NP_851830.1:n.452-144G>T
NR_024048.2:n.925+142G>T
XM_006724836.1:c.637+142G>T	XP_006724899.1:n.637+142G>T
XM_006724837.1:c.506-144G>T	XP_006724900.1:n.506-144G>T
XM_006724839.1:c.506-144G>T	XP_006724902.1:n.506-144G>T
XM_006724841.2:c.376+142G>T	XP_006724904.1:n.376+142G>T
XM_006724842.2:c.286+142G>T	XP_006724905.1:n.286+142G>T
XM_011531189.1:c.425-144G>T	XP_011529491.1:n.425-144G>T
XM_011531190.1:c.376+142G>T	XP_011529492.1:n.376+142G>T
XM_011531191.1:c.307+142G>T	XP_011529493.1:n.307+142G>T
XM_011531192.1:c.304+142G>T	XP_011529494.1:n.304+142G>T
XR_938511.1:n.931+142G>T
XM_006724841.4:c.376+142G>T	XP_006724904.1:n.376+142G>T
XM_006724842.4:c.286+142G>T	XP_006724905.1:n.286+142G>T
XM_011531191.2:c.307+142G>T	XP_011529493.1:n.307+142G>T
XM_017029761.1:c.452-144G>T	XP_016885250.1:n.452-144G>T
XM_017029762.1:c.547+142G>T	XP_016885251.1:n.547+142G>T
XM_017029763.1:c.371-144G>T	XP_016885252.1:n.371-144G>T
XM_017029764.1:c.304+142G>T	XP_016885253.1:n.304+142G>T
XM_017029765.2:c.245-144G>T	XP_016885254.1:n.245-144G>T
XM_024452431.1:c.425-144G>T	XP_024308199.1:n.425-144G>T
NM_000116.5:c.583+142G>T MANE Select	NP_000107.1:n.583+142G>T
NM_001303465.2:c.596-144G>T	NP_001290394.1:n.596-144G>T
NM_181311.4:c.493+142G>T	NP_851828.1:n.493+142G>T
NM_181312.4:c.542-144G>T	NP_851829.1:n.542-144G>T
NM_181313.4:c.452-144G>T	NP_851830.1:n.452-144G>T
NR_024048.3:n.904+142G>T