Canonical Allele Identifier: CA415185144

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153648571A>G (hg19) ; chrX:g.154420232A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420232A>G , CM000685.2:g.154420232A>G	GRCh38
NC_000023.10:g.153648571A>G , CM000685.1:g.153648571A>G	GRCh37
NC_000023.9:g.153301765A>G	NCBI36
NG_009634.1:g.13695A>G
NG_009634.2:g.13698A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1477A>G
ENST00000698317.1:n.2093A>G
ENST00000698318.1:n.1876A>G
ENST00000698319.1:n.1239A>G
ENST00000698320.1:n.1127A>G
ENST00000470127.2:n.1140A>G
ENST00000475699.6:c.631A>G	ENSP00000419854.3:p.Asn211Asp
ENST00000483674.3:n.549A>G
ENST00000601016.6:c.667A>G MANE Select	ENSP00000469981.1:p.Asn223Asp
ENST00000612012.5:c.625A>G	ENSP00000482070.2:p.Asn209Asp
ENST00000612460.5:c.577A>G	ENSP00000481037.1:p.Asn193Asp
ENST00000614595.2:n.2014A>G
ENST00000615658.5:n.1256A>G
ENST00000616020.5:c.679A>G	ENSP00000483636.2:p.Asn227Asp
ENST00000617701.5:c.*680A>G	ENSP00000481645.1:n.*680A>G
ENST00000652354.1:c.349A>G	ENSP00000498734.1:p.Asn117Asp
ENST00000652358.1:c.460A>G	ENSP00000498464.1:p.Asn154Asp
ENST00000652390.1:c.586A>G	ENSP00000498858.1:p.Asn196Asp
ENST00000652476.1:n.1333A>G
ENST00000652644.1:c.280A>G	ENSP00000498496.1:p.Asn94Asp
ENST00000652682.1:c.724A>G	ENSP00000498288.1:p.Asn242Asp
ENST00000652685.1:n.1020A>G
ENST00000369776.8:c.577A>G	ENSP00000358791.4:p.Asn193Asp
ENST00000426231.5:c.664A>G
ENST00000475699.5:c.625A>G	ENSP00000419854.2:p.Asn209Asp
ENST00000494912.5:n.1356A>G
ENST00000498029.1:n.125A>G
ENST00000601016.5:c.667A>G	ENSP00000469981.1:p.Asn223Asp
ENST00000612460.4:c.577A>G	ENSP00000481037.1:p.Asn193Asp
ENST00000613002.4:c.535A>G	ENSP00000478154.1:p.Asn179Asp
ENST00000615986.4:c.*395A>G	ENSP00000480133.1:n.*395A>G
NM_000116.4:c.667A>G	NP_000107.1:p.Asn223Asp
NM_001303465.1:c.679A>G	NP_001290394.1:p.Asn227Asp
NM_181311.3:c.577A>G	NP_851828.1:p.Asn193Asp
NM_181312.3:c.625A>G	NP_851829.1:p.Asn209Asp
NM_181313.3:c.535A>G	NP_851830.1:p.Asn179Asp
NR_024048.2:n.1009A>G
XM_006724836.1:c.721A>G	XP_006724899.1:p.Asn241Asp
XM_006724837.1:c.706A>G	XP_006724900.1:p.Asn236Asp
XM_006724839.1:c.589A>G	XP_006724902.1:p.Asn197Asp
XM_006724841.2:c.460A>G	XP_006724904.1:p.Asn154Asp
XM_006724842.2:c.370A>G	XP_006724905.1:p.Asn124Asp
XM_011531189.1:c.508A>G	XP_011529491.1:p.Asn170Asp
XM_011531190.1:c.460A>G	XP_011529492.1:p.Asn154Asp
XM_011531191.1:c.391A>G	XP_011529493.1:p.Asn131Asp
XM_011531192.1:c.388A>G	XP_011529494.1:p.Asn130Asp
XR_938511.1:n.1015A>G
XM_006724841.4:c.460A>G	XP_006724904.1:p.Asn154Asp
XM_006724842.4:c.370A>G	XP_006724905.1:p.Asn124Asp
XM_011531191.2:c.391A>G	XP_011529493.1:p.Asn131Asp
XM_017029761.1:c.652A>G	XP_016885250.1:p.Asn218Asp
XM_017029762.1:c.631A>G	XP_016885251.1:p.Asn211Asp
XM_017029763.1:c.454A>G	XP_016885252.1:p.Asn152Asp
XM_017029764.1:c.388A>G	XP_016885253.1:p.Asn130Asp
XM_017029765.2:c.328A>G	XP_016885254.1:p.Asn110Asp
XM_024452431.1:c.625A>G	XP_024308199.1:p.Asn209Asp
NM_000116.5:c.667A>G MANE Select	NP_000107.1:p.Asn223Asp
NM_001303465.2:c.679A>G	NP_001290394.1:p.Asn227Asp
NM_181311.4:c.577A>G	NP_851828.1:p.Asn193Asp
NM_181312.4:c.625A>G	NP_851829.1:p.Asn209Asp
NM_181313.4:c.535A>G	NP_851830.1:p.Asn179Asp
NR_024048.3:n.988A>G