Canonical Allele Identifier: CA415185161

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153648574A>G (hg19) ; chrX:g.154420235A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420235A>G , CM000685.2:g.154420235A>G	GRCh38
NC_000023.10:g.153648574A>G , CM000685.1:g.153648574A>G	GRCh37
NC_000023.9:g.153301768A>G	NCBI36
NG_009634.1:g.13698A>G
NG_009634.2:g.13701A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1480A>G
ENST00000698317.1:n.2096A>G
ENST00000698318.1:n.1879A>G
ENST00000698319.1:n.1242A>G
ENST00000698320.1:n.1130A>G
ENST00000470127.2:n.1143A>G
ENST00000475699.6:c.634A>G	ENSP00000419854.3:p.Ser212Gly
ENST00000483674.3:n.552A>G
ENST00000601016.6:c.670A>G MANE Select	ENSP00000469981.1:p.Ser224Gly
ENST00000612012.5:c.628A>G	ENSP00000482070.2:p.Ser210Gly
ENST00000612460.5:c.580A>G	ENSP00000481037.1:p.Ser194Gly
ENST00000614595.2:n.2017A>G
ENST00000615658.5:n.1259A>G
ENST00000616020.5:c.682A>G	ENSP00000483636.2:p.Ser228Gly
ENST00000617701.5:c.*683A>G	ENSP00000481645.1:n.*683A>G
ENST00000652354.1:c.352A>G	ENSP00000498734.1:p.Ser118Gly
ENST00000652358.1:c.463A>G	ENSP00000498464.1:p.Ser155Gly
ENST00000652390.1:c.589A>G	ENSP00000498858.1:p.Ser197Gly
ENST00000652476.1:n.1336A>G
ENST00000652644.1:c.283A>G	ENSP00000498496.1:p.Ser95Gly
ENST00000652682.1:c.727A>G	ENSP00000498288.1:p.Ser243Gly
ENST00000652685.1:n.1023A>G
ENST00000369776.8:c.580A>G	ENSP00000358791.4:p.Ser194Gly
ENST00000426231.5:c.667A>G
ENST00000475699.5:c.628A>G	ENSP00000419854.2:p.Ser210Gly
ENST00000494912.5:n.1359A>G
ENST00000498029.1:n.128A>G
ENST00000601016.5:c.670A>G	ENSP00000469981.1:p.Ser224Gly
ENST00000612460.4:c.580A>G	ENSP00000481037.1:p.Ser194Gly
ENST00000613002.4:c.538A>G	ENSP00000478154.1:p.Ser180Gly
ENST00000615986.4:c.*398A>G	ENSP00000480133.1:n.*398A>G
NM_000116.4:c.670A>G	NP_000107.1:p.Ser224Gly
NM_001303465.1:c.682A>G	NP_001290394.1:p.Ser228Gly
NM_181311.3:c.580A>G	NP_851828.1:p.Ser194Gly
NM_181312.3:c.628A>G	NP_851829.1:p.Ser210Gly
NM_181313.3:c.538A>G	NP_851830.1:p.Ser180Gly
NR_024048.2:n.1012A>G
XM_006724836.1:c.724A>G	XP_006724899.1:p.Ser242Gly
XM_006724837.1:c.709A>G	XP_006724900.1:p.Ser237Gly
XM_006724839.1:c.592A>G	XP_006724902.1:p.Ser198Gly
XM_006724841.2:c.463A>G	XP_006724904.1:p.Ser155Gly
XM_006724842.2:c.373A>G	XP_006724905.1:p.Ser125Gly
XM_011531189.1:c.511A>G	XP_011529491.1:p.Ser171Gly
XM_011531190.1:c.463A>G	XP_011529492.1:p.Ser155Gly
XM_011531191.1:c.394A>G	XP_011529493.1:p.Ser132Gly
XM_011531192.1:c.391A>G	XP_011529494.1:p.Ser131Gly
XR_938511.1:n.1018A>G
XM_006724841.4:c.463A>G	XP_006724904.1:p.Ser155Gly
XM_006724842.4:c.373A>G	XP_006724905.1:p.Ser125Gly
XM_011531191.2:c.394A>G	XP_011529493.1:p.Ser132Gly
XM_017029761.1:c.655A>G	XP_016885250.1:p.Ser219Gly
XM_017029762.1:c.634A>G	XP_016885251.1:p.Ser212Gly
XM_017029763.1:c.457A>G	XP_016885252.1:p.Ser153Gly
XM_017029764.1:c.391A>G	XP_016885253.1:p.Ser131Gly
XM_017029765.2:c.331A>G	XP_016885254.1:p.Ser111Gly
XM_024452431.1:c.628A>G	XP_024308199.1:p.Ser210Gly
NM_000116.5:c.670A>G MANE Select	NP_000107.1:p.Ser224Gly
NM_001303465.2:c.682A>G	NP_001290394.1:p.Ser228Gly
NM_181311.4:c.580A>G	NP_851828.1:p.Ser194Gly
NM_181312.4:c.628A>G	NP_851829.1:p.Ser210Gly
NM_181313.4:c.538A>G	NP_851830.1:p.Ser180Gly
NR_024048.3:n.991A>G