Canonical Allele Identifier: CA415185170

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153648576T>G (hg19) ; chrX:g.154420237T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420237T>G , CM000685.2:g.154420237T>G	GRCh38
NC_000023.10:g.153648576T>G , CM000685.1:g.153648576T>G	GRCh37
NC_000023.9:g.153301770T>G	NCBI36
NG_009634.1:g.13700T>G
NG_009634.2:g.13703T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1482T>G
ENST00000698317.1:n.2098T>G
ENST00000698318.1:n.1881T>G
ENST00000698319.1:n.1244T>G
ENST00000698320.1:n.1132T>G
ENST00000470127.2:n.1145T>G
ENST00000475699.6:c.636T>G	ENSP00000419854.3:p.Ser212Arg
ENST00000483674.3:n.554T>G
ENST00000601016.6:c.672T>G MANE Select	ENSP00000469981.1:p.Ser224Arg
ENST00000612012.5:c.630T>G	ENSP00000482070.2:p.Ser210Arg
ENST00000612460.5:c.582T>G	ENSP00000481037.1:p.Ser194Arg
ENST00000614595.2:n.2019T>G
ENST00000615658.5:n.1261T>G
ENST00000616020.5:c.684T>G	ENSP00000483636.2:p.Ser228Arg
ENST00000617701.5:c.*685T>G	ENSP00000481645.1:n.*685T>G
ENST00000652354.1:c.354T>G	ENSP00000498734.1:p.Ser118Arg
ENST00000652358.1:c.465T>G	ENSP00000498464.1:p.Ser155Arg
ENST00000652390.1:c.591T>G	ENSP00000498858.1:p.Ser197Arg
ENST00000652476.1:n.1338T>G
ENST00000652644.1:c.285T>G	ENSP00000498496.1:p.Ser95Arg
ENST00000652682.1:c.729T>G	ENSP00000498288.1:p.Ser243Arg
ENST00000652685.1:n.1025T>G
ENST00000369776.8:c.582T>G	ENSP00000358791.4:p.Ser194Arg
ENST00000426231.5:c.669T>G
ENST00000475699.5:c.630T>G	ENSP00000419854.2:p.Ser210Arg
ENST00000494912.5:n.1361T>G
ENST00000498029.1:n.130T>G
ENST00000601016.5:c.672T>G	ENSP00000469981.1:p.Ser224Arg
ENST00000612460.4:c.582T>G	ENSP00000481037.1:p.Ser194Arg
ENST00000613002.4:c.540T>G	ENSP00000478154.1:p.Ser180Arg
ENST00000615986.4:c.*400T>G	ENSP00000480133.1:n.*400T>G
NM_000116.4:c.672T>G	NP_000107.1:p.Ser224Arg
NM_001303465.1:c.684T>G	NP_001290394.1:p.Ser228Arg
NM_181311.3:c.582T>G	NP_851828.1:p.Ser194Arg
NM_181312.3:c.630T>G	NP_851829.1:p.Ser210Arg
NM_181313.3:c.540T>G	NP_851830.1:p.Ser180Arg
NR_024048.2:n.1014T>G
XM_006724836.1:c.726T>G	XP_006724899.1:p.Ser242Arg
XM_006724837.1:c.711T>G	XP_006724900.1:p.Ser237Arg
XM_006724839.1:c.594T>G	XP_006724902.1:p.Ser198Arg
XM_006724841.2:c.465T>G	XP_006724904.1:p.Ser155Arg
XM_006724842.2:c.375T>G	XP_006724905.1:p.Ser125Arg
XM_011531189.1:c.513T>G	XP_011529491.1:p.Ser171Arg
XM_011531190.1:c.465T>G	XP_011529492.1:p.Ser155Arg
XM_011531191.1:c.396T>G	XP_011529493.1:p.Ser132Arg
XM_011531192.1:c.393T>G	XP_011529494.1:p.Ser131Arg
XR_938511.1:n.1020T>G
XM_006724841.4:c.465T>G	XP_006724904.1:p.Ser155Arg
XM_006724842.4:c.375T>G	XP_006724905.1:p.Ser125Arg
XM_011531191.2:c.396T>G	XP_011529493.1:p.Ser132Arg
XM_017029761.1:c.657T>G	XP_016885250.1:p.Ser219Arg
XM_017029762.1:c.636T>G	XP_016885251.1:p.Ser212Arg
XM_017029763.1:c.459T>G	XP_016885252.1:p.Ser153Arg
XM_017029764.1:c.393T>G	XP_016885253.1:p.Ser131Arg
XM_017029765.2:c.333T>G	XP_016885254.1:p.Ser111Arg
XM_024452431.1:c.630T>G	XP_024308199.1:p.Ser210Arg
NM_000116.5:c.672T>G MANE Select	NP_000107.1:p.Ser224Arg
NM_001303465.2:c.684T>G	NP_001290394.1:p.Ser228Arg
NM_181311.4:c.582T>G	NP_851828.1:p.Ser194Arg
NM_181312.4:c.630T>G	NP_851829.1:p.Ser210Arg
NM_181313.4:c.540T>G	NP_851830.1:p.Ser180Arg
NR_024048.3:n.993T>G