Canonical Allele Identifier: CA415185084

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153648556A>T (hg19) ; chrX:g.154420217A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420217A>T , CM000685.2:g.154420217A>T	GRCh38
NC_000023.10:g.153648556A>T , CM000685.1:g.153648556A>T	GRCh37
NC_000023.9:g.153301750A>T	NCBI36
NG_009634.1:g.13680A>T
NG_009634.2:g.13683A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.1462A>T
ENST00000698317.1:n.2078A>T
ENST00000698318.1:n.1861A>T
ENST00000698319.1:n.1224A>T
ENST00000698320.1:n.1112A>T
ENST00000470127.2:n.1125A>T
ENST00000475699.6:c.616A>T	ENSP00000419854.3:p.Asn206Tyr
ENST00000483674.3:n.534A>T
ENST00000601016.6:c.652A>T MANE Select	ENSP00000469981.1:p.Asn218Tyr
ENST00000612012.5:c.610A>T	ENSP00000482070.2:p.Asn204Tyr
ENST00000612460.5:c.562A>T	ENSP00000481037.1:p.Asn188Tyr
ENST00000614595.2:n.1999A>T
ENST00000615658.5:n.1241A>T
ENST00000616020.5:c.664A>T	ENSP00000483636.2:p.Asn222Tyr
ENST00000617701.5:c.*665A>T	ENSP00000481645.1:n.*665A>T
ENST00000652354.1:c.334A>T	ENSP00000498734.1:p.Asn112Tyr
ENST00000652358.1:c.445A>T	ENSP00000498464.1:p.Asn149Tyr
ENST00000652390.1:c.571A>T	ENSP00000498858.1:p.Asn191Tyr
ENST00000652476.1:n.1318A>T
ENST00000652644.1:c.265A>T	ENSP00000498496.1:p.Asn89Tyr
ENST00000652682.1:c.709A>T	ENSP00000498288.1:p.Asn237Tyr
ENST00000652685.1:n.1005A>T
ENST00000369776.8:c.562A>T	ENSP00000358791.4:p.Asn188Tyr
ENST00000426231.5:c.649A>T
ENST00000475699.5:c.610A>T	ENSP00000419854.2:p.Asn204Tyr
ENST00000494912.5:n.1341A>T
ENST00000498029.1:n.110A>T
ENST00000601016.5:c.652A>T	ENSP00000469981.1:p.Asn218Tyr
ENST00000612460.4:c.562A>T	ENSP00000481037.1:p.Asn188Tyr
ENST00000613002.4:c.520A>T	ENSP00000478154.1:p.Asn174Tyr
ENST00000615986.4:c.*380A>T	ENSP00000480133.1:n.*380A>T
NM_000116.4:c.652A>T	NP_000107.1:p.Asn218Tyr
NM_001303465.1:c.664A>T	NP_001290394.1:p.Asn222Tyr
NM_181311.3:c.562A>T	NP_851828.1:p.Asn188Tyr
NM_181312.3:c.610A>T	NP_851829.1:p.Asn204Tyr
NM_181313.3:c.520A>T	NP_851830.1:p.Asn174Tyr
NR_024048.2:n.994A>T
XM_006724836.1:c.706A>T	XP_006724899.1:p.Asn236Tyr
XM_006724837.1:c.691A>T	XP_006724900.1:p.Asn231Tyr
XM_006724839.1:c.574A>T	XP_006724902.1:p.Asn192Tyr
XM_006724841.2:c.445A>T	XP_006724904.1:p.Asn149Tyr
XM_006724842.2:c.355A>T	XP_006724905.1:p.Asn119Tyr
XM_011531189.1:c.493A>T	XP_011529491.1:p.Asn165Tyr
XM_011531190.1:c.445A>T	XP_011529492.1:p.Asn149Tyr
XM_011531191.1:c.376A>T	XP_011529493.1:p.Asn126Tyr
XM_011531192.1:c.373A>T	XP_011529494.1:p.Asn125Tyr
XR_938511.1:n.1000A>T
XM_006724841.4:c.445A>T	XP_006724904.1:p.Asn149Tyr
XM_006724842.4:c.355A>T	XP_006724905.1:p.Asn119Tyr
XM_011531191.2:c.376A>T	XP_011529493.1:p.Asn126Tyr
XM_017029761.1:c.637A>T	XP_016885250.1:p.Asn213Tyr
XM_017029762.1:c.616A>T	XP_016885251.1:p.Asn206Tyr
XM_017029763.1:c.439A>T	XP_016885252.1:p.Asn147Tyr
XM_017029764.1:c.373A>T	XP_016885253.1:p.Asn125Tyr
XM_017029765.2:c.313A>T	XP_016885254.1:p.Asn105Tyr
XM_024452431.1:c.610A>T	XP_024308199.1:p.Asn204Tyr
NM_000116.5:c.652A>T MANE Select	NP_000107.1:p.Asn218Tyr
NM_001303465.2:c.664A>T	NP_001290394.1:p.Asn222Tyr
NM_181311.4:c.562A>T	NP_851828.1:p.Asn188Tyr
NM_181312.4:c.610A>T	NP_851829.1:p.Asn204Tyr
NM_181313.4:c.520A>T	NP_851830.1:p.Asn174Tyr
NR_024048.3:n.973A>T