Canonical Allele Identifier: CA415184418

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153648427C>G (hg19) ; chrX:g.154420088C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420088C>G , CM000685.2:g.154420088C>G	GRCh38
NC_000023.10:g.153648427C>G , CM000685.1:g.153648427C>G	GRCh37
NC_000023.9:g.153301621C>G	NCBI36
NG_009634.1:g.13551C>G
NG_009634.2:g.13554C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1450C>G
ENST00000698317.1:n.2066C>G
ENST00000698318.1:n.1849C>G
ENST00000698319.1:n.1212C>G
ENST00000698320.1:n.1100C>G
ENST00000470127.2:n.1113C>G
ENST00000475699.6:c.604C>G	ENSP00000419854.3:p.His202Asp
ENST00000483674.3:n.522C>G
ENST00000601016.6:c.640C>G MANE Select	ENSP00000469981.1:p.His214Asp
ENST00000612012.5:c.598C>G	ENSP00000482070.2:p.His200Asp
ENST00000612460.5:c.550C>G	ENSP00000481037.1:p.His184Asp
ENST00000614595.2:n.1987C>G
ENST00000615658.5:n.1229C>G
ENST00000616020.5:c.652C>G	ENSP00000483636.2:p.His218Asp
ENST00000617701.5:c.*653C>G	ENSP00000481645.1:n.*653C>G
ENST00000652354.1:c.322C>G	ENSP00000498734.1:p.His108Asp
ENST00000652358.1:c.433C>G	ENSP00000498464.1:p.His145Asp
ENST00000652390.1:c.559C>G	ENSP00000498858.1:p.His187Asp
ENST00000652476.1:n.1306C>G
ENST00000652644.1:c.253C>G	ENSP00000498496.1:p.His85Asp
ENST00000652682.1:c.697C>G	ENSP00000498288.1:p.His233Asp
ENST00000652685.1:n.993C>G
ENST00000369776.8:c.433C>G	ENSP00000358791.4:p.His145Asp
ENST00000426231.5:c.637C>G
ENST00000439735.2:c.547C>G	ENSP00000398193.1:p.His183Asp
ENST00000470127.1:n.219C>G
ENST00000475699.5:c.598C>G	ENSP00000419854.2:p.His200Asp
ENST00000494912.5:n.1329C>G
ENST00000498029.1:n.98C>G
ENST00000601016.5:c.640C>G	ENSP00000469981.1:p.His214Asp
ENST00000612460.4:c.550C>G	ENSP00000481037.1:p.His184Asp
ENST00000613002.4:c.508C>G	ENSP00000478154.1:p.His170Asp
ENST00000615986.4:c.*368C>G	ENSP00000480133.1:n.*368C>G
NM_000116.4:c.640C>G	NP_000107.1:p.His214Asp
NM_001303465.1:c.652C>G	NP_001290394.1:p.His218Asp
NM_181311.3:c.550C>G	NP_851828.1:p.His184Asp
NM_181312.3:c.598C>G	NP_851829.1:p.His200Asp
NM_181313.3:c.508C>G	NP_851830.1:p.His170Asp
NR_024048.2:n.982C>G
XM_006724836.1:c.694C>G	XP_006724899.1:p.His232Asp
XM_006724837.1:c.562C>G	XP_006724900.1:p.His188Asp
XM_006724839.1:c.562C>G	XP_006724902.1:p.His188Asp
XM_006724841.2:c.433C>G	XP_006724904.1:p.His145Asp
XM_006724842.2:c.343C>G	XP_006724905.1:p.His115Asp
XM_011531189.1:c.481C>G	XP_011529491.1:p.His161Asp
XM_011531190.1:c.433C>G	XP_011529492.1:p.His145Asp
XM_011531191.1:c.364C>G	XP_011529493.1:p.His122Asp
XM_011531192.1:c.361C>G	XP_011529494.1:p.His121Asp
XR_938511.1:n.988C>G
XM_006724841.4:c.433C>G	XP_006724904.1:p.His145Asp
XM_006724842.4:c.343C>G	XP_006724905.1:p.His115Asp
XM_011531191.2:c.364C>G	XP_011529493.1:p.His122Asp
XM_017029761.1:c.508C>G	XP_016885250.1:p.His170Asp
XM_017029762.1:c.604C>G	XP_016885251.1:p.His202Asp
XM_017029763.1:c.427C>G	XP_016885252.1:p.His143Asp
XM_017029764.1:c.361C>G	XP_016885253.1:p.His121Asp
XM_017029765.2:c.301C>G	XP_016885254.1:p.His101Asp
XM_024452431.1:c.481C>G	XP_024308199.1:p.His161Asp
NM_000116.5:c.640C>G MANE Select	NP_000107.1:p.His214Asp
NM_001303465.2:c.652C>G	NP_001290394.1:p.His218Asp
NM_181311.4:c.550C>G	NP_851828.1:p.His184Asp
NM_181312.4:c.598C>G	NP_851829.1:p.His200Asp
NM_181313.4:c.508C>G	NP_851830.1:p.His170Asp
NR_024048.3:n.961C>G