Canonical Allele Identifier: CA415181163

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153641854A>C (hg19) ; chrX:g.154413517A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413517A>C , CM000685.2:g.154413517A>C	GRCh38
NC_000023.10:g.153641854A>C , CM000685.1:g.153641854A>C	GRCh37
NC_000023.9:g.153295048A>C	NCBI36
NG_009634.1:g.6978A>C
NG_012884.2:g.3572T>G
NG_009634.2:g.6983A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.854A>C
ENST00000698235.1:n.394A>C
ENST00000698317.1:n.1380A>C
ENST00000698318.1:n.1253A>C
ENST00000470127.2:n.598A>C
ENST00000475699.6:c.374A>C	ENSP00000419854.3:p.Glu125Ala
ENST00000476800.2:n.1506A>C
ENST00000483674.3:n.211A>C
ENST00000601016.6:c.320A>C MANE Select	ENSP00000469981.1:p.Glu107Ala
ENST00000612012.5:c.320A>C	ENSP00000482070.2:p.Glu107Ala
ENST00000612460.5:c.320A>C	ENSP00000481037.1:p.Glu107Ala
ENST00000614595.2:n.1757A>C
ENST00000615658.5:n.633A>C
ENST00000616020.5:c.374A>C	ENSP00000483636.2:p.Glu125Ala
ENST00000617701.5:c.*138A>C	ENSP00000481645.1:n.*138A>C
ENST00000621647.2:n.602A>C
ENST00000652354.1:c.44A>C	ENSP00000498734.1:p.Glu15Ala
ENST00000652358.1:c.113A>C	ENSP00000498464.1:p.Glu38Ala
ENST00000652390.1:c.239A>C	ENSP00000498858.1:p.Glu80Ala
ENST00000652476.1:n.710A>C
ENST00000652682.1:c.320A>C	ENSP00000498288.1:p.Glu107Ala
ENST00000652685.1:n.478A>C
ENST00000369776.8:c.245A>C	ENSP00000358791.4:p.Glu82Ala
ENST00000426231.5:c.236A>C
ENST00000439735.2:c.320A>C	ENSP00000398193.1:p.Glu107Ala
ENST00000475699.5:c.320A>C	ENSP00000419854.2:p.Glu107Ala
ENST00000476679.5:n.233A>C
ENST00000476800.1:n.427A>C
ENST00000479875.1:n.349A>C
ENST00000483674.2:n.29A>C
ENST00000483780.5:n.94A>C
ENST00000601016.5:c.320A>C	ENSP00000469981.1:p.Glu107Ala
ENST00000612012.4:c.374A>C	ENSP00000482070.1:p.Glu125Ala
ENST00000612460.4:c.320A>C	ENSP00000481037.1:p.Glu107Ala
ENST00000613002.4:c.320A>C	ENSP00000478154.1:p.Glu107Ala
ENST00000613634.4:n.640A>C
ENST00000615658.4:n.733A>C
ENST00000615986.4:c.*138A>C	ENSP00000480133.1:n.*138A>C
ENST00000616020.4:c.374A>C	ENSP00000483636.1:p.Glu125Ala
ENST00000617701.4:c.*150A>C	ENSP00000481645.1:n.*150A>C
ENST00000620808.4:c.*119A>C	ENSP00000479311.1:n.*119A>C
ENST00000621647.1:n.834A>C
NM_000116.4:c.320A>C	NP_000107.1:p.Glu107Ala
NM_001303465.1:c.374A>C	NP_001290394.1:p.Glu125Ala
NM_181311.3:c.320A>C	NP_851828.1:p.Glu107Ala
NM_181312.3:c.320A>C	NP_851829.1:p.Glu107Ala
NM_181313.3:c.320A>C	NP_851830.1:p.Glu107Ala
NR_024048.2:n.752A>C
XM_006724836.1:c.374A>C	XP_006724899.1:p.Glu125Ala
XM_006724837.1:c.374A>C	XP_006724900.1:p.Glu125Ala
XM_006724839.1:c.374A>C	XP_006724902.1:p.Glu125Ala
XM_006724841.2:c.113A>C	XP_006724904.1:p.Glu38Ala
XM_006724842.2:c.113A>C	XP_006724905.1:p.Glu38Ala
XM_011531189.1:c.374A>C	XP_011529491.1:p.Glu125Ala
XM_011531190.1:c.113A>C	XP_011529492.1:p.Glu38Ala
XM_011531191.1:c.44A>C	XP_011529493.1:p.Glu15Ala
XM_011531192.1:c.41A>C	XP_011529494.1:p.Glu14Ala
XR_938511.1:n.677A>C
XM_006724841.4:c.113A>C	XP_006724904.1:p.Glu38Ala
XM_006724842.4:c.113A>C	XP_006724905.1:p.Glu38Ala
XM_011531191.2:c.44A>C	XP_011529493.1:p.Glu15Ala
XM_017029761.1:c.320A>C	XP_016885250.1:p.Glu107Ala
XM_017029762.1:c.374A>C	XP_016885251.1:p.Glu125Ala
XM_017029763.1:c.320A>C	XP_016885252.1:p.Glu107Ala
XM_017029764.1:c.41A>C	XP_016885253.1:p.Glu14Ala
XM_017029765.2:c.113A>C	XP_016885254.1:p.Glu38Ala
XM_024452431.1:c.374A>C	XP_024308199.1:p.Glu125Ala
NM_000116.5:c.320A>C MANE Select	NP_000107.1:p.Glu107Ala
NM_001303465.2:c.374A>C	NP_001290394.1:p.Glu125Ala
NM_181311.4:c.320A>C	NP_851828.1:p.Glu107Ala
NM_181312.4:c.320A>C	NP_851829.1:p.Glu107Ala
NM_181313.4:c.320A>C	NP_851830.1:p.Glu107Ala
NR_024048.3:n.731A>C