Canonical Allele Identifier: CA2466677584

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420094G= , CM000685.2:g.154420094G=	GRCh38
NC_000023.10:g.153648433G= , CM000685.1:g.153648433G=	GRCh37
NC_000023.9:g.153301627G=	NCBI36
NG_009634.1:g.13557G=
NG_009634.2:g.13560G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1456G=
ENST00000698317.1:n.2072G=
ENST00000698318.1:n.1855G=
ENST00000698319.1:n.1218G=
ENST00000698320.1:n.1106G=
ENST00000470127.2:n.1119G=
ENST00000475699.6:c.610G=	ENSP00000419854.3:p.Gly204=
ENST00000483674.3:n.528G=
ENST00000601016.6:c.646G= MANE Select	ENSP00000469981.1:p.Gly216=
ENST00000612012.5:c.604G=	ENSP00000482070.2:p.Gly202=
ENST00000612460.5:c.556G=	ENSP00000481037.1:p.Gly186=
ENST00000614595.2:n.1993G=
ENST00000615658.5:n.1235G=
ENST00000616020.5:c.658G=	ENSP00000483636.2:p.Gly220=
ENST00000617701.5:c.*659G=	ENSP00000481645.1:n.*659G=
ENST00000652354.1:c.328G=	ENSP00000498734.1:p.Gly110=
ENST00000652358.1:c.439G=	ENSP00000498464.1:p.Gly147=
ENST00000652390.1:c.565G=	ENSP00000498858.1:p.Gly189=
ENST00000652476.1:n.1312G=
ENST00000652644.1:c.259G=	ENSP00000498496.1:p.Gly87=
ENST00000652682.1:c.703G=	ENSP00000498288.1:p.Gly235=
ENST00000652685.1:n.999G=
ENST00000369776.8:c.439G=	ENSP00000358791.4:p.Gly147=
ENST00000426231.5:c.643G=
ENST00000439735.2:c.553G=
ENST00000470127.1:n.225G=
ENST00000475699.5:c.604G=	ENSP00000419854.2:p.Gly202=
ENST00000494912.5:n.1335G=
ENST00000498029.1:n.104G=
ENST00000601016.5:c.646G=	ENSP00000469981.1:p.Gly216=
ENST00000612460.4:c.556G=	ENSP00000481037.1:p.Gly186=
ENST00000613002.4:c.514G=	ENSP00000478154.1:p.Gly172=
ENST00000615986.4:c.*374G=	ENSP00000480133.1:n.*374G=
NM_000116.4:c.646G=	NP_000107.1:p.Gly216=
NM_001303465.1:c.658G=	NP_001290394.1:p.Gly220=
NM_181311.3:c.556G=	NP_851828.1:p.Gly186=
NM_181312.3:c.604G=	NP_851829.1:p.Gly202=
NM_181313.3:c.514G=	NP_851830.1:p.Gly172=
NR_024048.2:n.988G=
XM_006724836.1:c.700G=	XP_006724899.1:p.Gly234=
XM_006724837.1:c.568G=	XP_006724900.1:p.Gly190=
XM_006724839.1:c.568G=	XP_006724902.1:p.Gly190=
XM_006724841.2:c.439G=	XP_006724904.1:p.Gly147=
XM_006724842.2:c.349G=	XP_006724905.1:p.Gly117=
XM_011531189.1:c.487G=	XP_011529491.1:p.Gly163=
XM_011531190.1:c.439G=	XP_011529492.1:p.Gly147=
XM_011531191.1:c.370G=	XP_011529493.1:p.Gly124=
XM_011531192.1:c.367G=	XP_011529494.1:p.Gly123=
XR_938511.1:n.994G=
XM_006724841.4:c.439G=	XP_006724904.1:p.Gly147=
XM_006724842.4:c.349G=	XP_006724905.1:p.Gly117=
XM_011531191.2:c.370G=	XP_011529493.1:p.Gly124=
XM_017029761.1:c.514G=	XP_016885250.1:p.Gly172=
XM_017029762.1:c.610G=	XP_016885251.1:p.Gly204=
XM_017029763.1:c.433G=	XP_016885252.1:p.Gly145=
XM_017029764.1:c.367G=	XP_016885253.1:p.Gly123=
XM_017029765.2:c.307G=	XP_016885254.1:p.Gly103=
XM_024452431.1:c.487G=	XP_024308199.1:p.Gly163=
NM_000116.5:c.646G= MANE Select	NP_000107.1:p.Gly216=
NM_001303465.2:c.658G=	NP_001290394.1:p.Gly220=
NM_181311.4:c.556G=	NP_851828.1:p.Gly186=
NM_181312.4:c.604G=	NP_851829.1:p.Gly202=
NM_181313.4:c.514G=	NP_851830.1:p.Gly172=
NR_024048.3:n.967G=