Canonical Allele Identifier: CA415180102

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153640531T>C (hg19) ; chrX:g.154412194T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154412194T>C , CM000685.2:g.154412194T>C	GRCh38
NC_000023.10:g.153640531T>C , CM000685.1:g.153640531T>C	GRCh37
NC_000023.9:g.153293725T>C	NCBI36
NG_009634.1:g.5655T>C
NG_012884.2:g.4895A>G
NG_009634.2:g.5660T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.646T>C
ENST00000698235.1:n.205T>C
ENST00000698317.1:n.180T>C
ENST00000698318.1:n.41T>C
ENST00000475699.6:c.272T>C	ENSP00000419854.3:p.Met91Thr
ENST00000476800.2:n.183T>C
ENST00000483674.3:n.109T>C
ENST00000601016.6:c.218T>C MANE Select	ENSP00000469981.1:p.Met73Thr
ENST00000612012.5:c.218T>C	ENSP00000482070.2:p.Met73Thr
ENST00000612460.5:c.218T>C	ENSP00000481037.1:p.Met73Thr
ENST00000614595.2:n.576T>C
ENST00000615658.5:n.531T>C
ENST00000616020.5:c.272T>C	ENSP00000483636.2:p.Met91Thr
ENST00000617701.5:c.218T>C	ENSP00000481645.1:p.Met73Thr
ENST00000621647.2:n.271T>C
ENST00000652358.1:c.-57+242T>C	ENSP00000498464.1:n.-57+242T>C
ENST00000652390.1:c.137T>C	ENSP00000498858.1:p.Met46Thr
ENST00000652476.1:n.379T>C
ENST00000652682.1:c.218T>C	ENSP00000498288.1:p.Met73Thr
ENST00000652685.1:n.270T>C
ENST00000369776.8:c.163+188T>C	ENSP00000358791.4:n.163+188T>C
ENST00000426231.5:c.34T>C
ENST00000439735.2:c.218T>C	ENSP00000398193.1:p.Met73Thr
ENST00000475699.5:c.218T>C	ENSP00000419854.2:p.Met73Thr
ENST00000601016.5:c.218T>C	ENSP00000469981.1:p.Met73Thr
ENST00000612012.4:c.272T>C	ENSP00000482070.1:p.Met91Thr
ENST00000612460.4:c.218T>C	ENSP00000481037.1:p.Met73Thr
ENST00000613002.4:c.218T>C	ENSP00000478154.1:p.Met73Thr
ENST00000613634.4:n.538T>C
ENST00000614595.1:n.437T>C
ENST00000615658.4:n.544T>C
ENST00000615986.4:c.218T>C	ENSP00000480133.1:p.Met73Thr
ENST00000616020.4:c.272T>C	ENSP00000483636.1:p.Met91Thr
ENST00000617701.4:c.218T>C	ENSP00000481645.1:p.Met73Thr
ENST00000620808.4:c.218T>C	ENSP00000479311.1:p.Met73Thr
ENST00000621647.1:n.503T>C
NM_000116.4:c.218T>C	NP_000107.1:p.Met73Thr
NM_001303465.1:c.272T>C	NP_001290394.1:p.Met91Thr
NM_181311.3:c.218T>C	NP_851828.1:p.Met73Thr
NM_181312.3:c.218T>C	NP_851829.1:p.Met73Thr
NM_181313.3:c.218T>C	NP_851830.1:p.Met73Thr
NR_024048.2:n.544T>C
XM_006724836.1:c.272T>C	XP_006724899.1:p.Met91Thr
XM_006724837.1:c.272T>C	XP_006724900.1:p.Met91Thr
XM_006724839.1:c.272T>C	XP_006724902.1:p.Met91Thr
XM_006724841.2:c.-77T>C	XP_006724904.1:n.-77T>C
XM_006724842.2:c.-77T>C	XP_006724905.1:n.-77T>C
XM_011531189.1:c.272T>C	XP_011529491.1:p.Met91Thr
XR_938511.1:n.575T>C
XM_006724841.4:c.-77T>C	XP_006724904.1:n.-77T>C
XM_006724842.4:c.-77T>C	XP_006724905.1:n.-77T>C
XM_017029761.1:c.218T>C	XP_016885250.1:p.Met73Thr
XM_017029762.1:c.272T>C	XP_016885251.1:p.Met91Thr
XM_017029763.1:c.218T>C	XP_016885252.1:p.Met73Thr
XM_017029765.2:c.-77T>C	XP_016885254.1:n.-77T>C
XM_024452431.1:c.272T>C	XP_024308199.1:p.Met91Thr
NM_000116.5:c.218T>C MANE Select	NP_000107.1:p.Met73Thr
NM_001303465.2:c.272T>C	NP_001290394.1:p.Met91Thr
NM_181311.4:c.218T>C	NP_851828.1:p.Met73Thr
NM_181312.4:c.218T>C	NP_851829.1:p.Met73Thr
NM_181313.4:c.218T>C	NP_851830.1:p.Met73Thr
NR_024048.3:n.523T>C