Canonical Allele Identifier: CA415182075

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153641890T>C (hg19) ; chrX:g.154413553T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413553T>C , CM000685.2:g.154413553T>C	GRCh38
NC_000023.10:g.153641890T>C , CM000685.1:g.153641890T>C	GRCh37
NC_000023.9:g.153295084T>C	NCBI36
NG_009634.1:g.7014T>C
NG_012884.2:g.3536A>G
NG_009634.2:g.7019T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.890T>C
ENST00000698235.1:n.430T>C
ENST00000698317.1:n.1416T>C
ENST00000698318.1:n.1289T>C
ENST00000470127.2:n.634T>C
ENST00000475699.6:c.410T>C	ENSP00000419854.3:p.Val137Ala
ENST00000476800.2:n.1542T>C
ENST00000483674.3:n.247T>C
ENST00000601016.6:c.356T>C MANE Select	ENSP00000469981.1:p.Val119Ala
ENST00000612012.5:c.356T>C	ENSP00000482070.2:p.Val119Ala
ENST00000612460.5:c.356T>C	ENSP00000481037.1:p.Val119Ala
ENST00000614595.2:n.1793T>C
ENST00000615658.5:n.669T>C
ENST00000616020.5:c.410T>C	ENSP00000483636.2:p.Val137Ala
ENST00000617701.5:c.*174T>C	ENSP00000481645.1:n.*174T>C
ENST00000621647.2:n.638T>C
ENST00000652354.1:c.80T>C	ENSP00000498734.1:p.Val27Ala
ENST00000652358.1:c.149T>C	ENSP00000498464.1:p.Val50Ala
ENST00000652390.1:c.275T>C	ENSP00000498858.1:p.Val92Ala
ENST00000652476.1:n.746T>C
ENST00000652644.1:c.2T>C	ENSP00000498496.1:p.Val1Ala
ENST00000652682.1:c.356T>C	ENSP00000498288.1:p.Val119Ala
ENST00000652685.1:n.514T>C
ENST00000369776.8:c.281T>C	ENSP00000358791.4:p.Val94Ala
ENST00000426231.5:c.272T>C
ENST00000439735.2:c.356T>C	ENSP00000398193.1:p.Val119Ala
ENST00000470127.1:n.25T>C
ENST00000475699.5:c.356T>C	ENSP00000419854.2:p.Val119Ala
ENST00000476679.5:n.269T>C
ENST00000476800.1:n.463T>C
ENST00000479875.1:n.385T>C
ENST00000483674.2:n.65T>C
ENST00000483780.5:n.130T>C
ENST00000601016.5:c.356T>C	ENSP00000469981.1:p.Val119Ala
ENST00000612012.4:c.410T>C	ENSP00000482070.1:p.Val137Ala
ENST00000612460.4:c.356T>C	ENSP00000481037.1:p.Val119Ala
ENST00000613002.4:c.356T>C	ENSP00000478154.1:p.Val119Ala
ENST00000613634.4:n.676T>C
ENST00000615658.4:n.769T>C
ENST00000615986.4:c.*174T>C	ENSP00000480133.1:n.*174T>C
ENST00000616020.4:c.410T>C	ENSP00000483636.1:p.Val137Ala
ENST00000617701.4:c.*186T>C	ENSP00000481645.1:n.*186T>C
ENST00000620808.4:c.*155T>C	ENSP00000479311.1:n.*155T>C
ENST00000621647.1:n.870T>C
NM_000116.4:c.356T>C	NP_000107.1:p.Val119Ala
NM_001303465.1:c.410T>C	NP_001290394.1:p.Val137Ala
NM_181311.3:c.356T>C	NP_851828.1:p.Val119Ala
NM_181312.3:c.356T>C	NP_851829.1:p.Val119Ala
NM_181313.3:c.356T>C	NP_851830.1:p.Val119Ala
NR_024048.2:n.788T>C
XM_006724836.1:c.410T>C	XP_006724899.1:p.Val137Ala
XM_006724837.1:c.410T>C	XP_006724900.1:p.Val137Ala
XM_006724839.1:c.410T>C	XP_006724902.1:p.Val137Ala
XM_006724841.2:c.149T>C	XP_006724904.1:p.Val50Ala
XM_006724842.2:c.149T>C	XP_006724905.1:p.Val50Ala
XM_011531189.1:c.410T>C	XP_011529491.1:p.Val137Ala
XM_011531190.1:c.149T>C	XP_011529492.1:p.Val50Ala
XM_011531191.1:c.80T>C	XP_011529493.1:p.Val27Ala
XM_011531192.1:c.77T>C	XP_011529494.1:p.Val26Ala
XR_938511.1:n.713T>C
XM_006724841.4:c.149T>C	XP_006724904.1:p.Val50Ala
XM_006724842.4:c.149T>C	XP_006724905.1:p.Val50Ala
XM_011531191.2:c.80T>C	XP_011529493.1:p.Val27Ala
XM_017029761.1:c.356T>C	XP_016885250.1:p.Val119Ala
XM_017029762.1:c.410T>C	XP_016885251.1:p.Val137Ala
XM_017029763.1:c.356T>C	XP_016885252.1:p.Val119Ala
XM_017029764.1:c.77T>C	XP_016885253.1:p.Val26Ala
XM_017029765.2:c.149T>C	XP_016885254.1:p.Val50Ala
XM_024452431.1:c.410T>C	XP_024308199.1:p.Val137Ala
NM_000116.5:c.356T>C MANE Select	NP_000107.1:p.Val119Ala
NM_001303465.2:c.410T>C	NP_001290394.1:p.Val137Ala
NM_181311.4:c.356T>C	NP_851828.1:p.Val119Ala
NM_181312.4:c.356T>C	NP_851829.1:p.Val119Ala
NM_181313.4:c.356T>C	NP_851830.1:p.Val119Ala
NR_024048.3:n.767T>C