Canonical Allele Identifier: CA415181004

Gene: TAFAZZIN

Linked Data

• MyVariant Identifiers: chrX:g.153641829G>T (hg19) ; chrX:g.154413492G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413492G>T , CM000685.2:g.154413492G>T	GRCh38
NC_000023.10:g.153641829G>T , CM000685.1:g.153641829G>T	GRCh37
NC_000023.9:g.153295023G>T	NCBI36
NG_009634.1:g.6953G>T
NG_012884.2:g.3597C>A
NG_009634.2:g.6958G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.829G>T
ENST00000698235.1:n.369G>T
ENST00000698317.1:n.1355G>T
ENST00000698318.1:n.1228G>T
ENST00000470127.2:n.573G>T
ENST00000475699.6:c.349G>T	ENSP00000419854.3:p.Ala117Ser
ENST00000476800.2:n.1481G>T
ENST00000483674.3:n.186G>T
ENST00000601016.6:c.295G>T MANE Select	ENSP00000469981.1:p.Ala99Ser
ENST00000612012.5:c.295G>T	ENSP00000482070.2:p.Ala99Ser
ENST00000612460.5:c.295G>T	ENSP00000481037.1:p.Ala99Ser
ENST00000614595.2:n.1732G>T
ENST00000615658.5:n.608G>T
ENST00000616020.5:c.349G>T	ENSP00000483636.2:p.Ala117Ser
ENST00000617701.5:c.*113G>T	ENSP00000481645.1:n.*113G>T
ENST00000621647.2:n.577G>T
ENST00000652354.1:c.19G>T	ENSP00000498734.1:p.Ala7Ser
ENST00000652358.1:c.88G>T	ENSP00000498464.1:p.Ala30Ser
ENST00000652390.1:c.214G>T	ENSP00000498858.1:p.Ala72Ser
ENST00000652476.1:n.685G>T
ENST00000652682.1:c.295G>T	ENSP00000498288.1:p.Ala99Ser
ENST00000652685.1:n.453G>T
ENST00000369776.8:c.220G>T	ENSP00000358791.4:p.Ala74Ser
ENST00000426231.5:c.211G>T
ENST00000439735.2:c.295G>T	ENSP00000398193.1:p.Ala99Ser
ENST00000475699.5:c.295G>T	ENSP00000419854.2:p.Ala99Ser
ENST00000476679.5:n.208G>T
ENST00000476800.1:n.402G>T
ENST00000479875.1:n.324G>T
ENST00000483674.2:n.4G>T
ENST00000483780.5:n.69G>T
ENST00000601016.5:c.295G>T	ENSP00000469981.1:p.Ala99Ser
ENST00000612012.4:c.349G>T	ENSP00000482070.1:p.Ala117Ser
ENST00000612460.4:c.295G>T	ENSP00000481037.1:p.Ala99Ser
ENST00000613002.4:c.295G>T	ENSP00000478154.1:p.Ala99Ser
ENST00000613634.4:n.615G>T
ENST00000615658.4:n.708G>T
ENST00000615986.4:c.*113G>T	ENSP00000480133.1:n.*113G>T
ENST00000616020.4:c.349G>T	ENSP00000483636.1:p.Ala117Ser
ENST00000617701.4:c.*125G>T	ENSP00000481645.1:n.*125G>T
ENST00000620808.4:c.*94G>T	ENSP00000479311.1:n.*94G>T
ENST00000621647.1:n.809G>T
NM_000116.4:c.295G>T	NP_000107.1:p.Ala99Ser
NM_001303465.1:c.349G>T	NP_001290394.1:p.Ala117Ser
NM_181311.3:c.295G>T	NP_851828.1:p.Ala99Ser
NM_181312.3:c.295G>T	NP_851829.1:p.Ala99Ser
NM_181313.3:c.295G>T	NP_851830.1:p.Ala99Ser
NR_024048.2:n.727G>T
XM_006724836.1:c.349G>T	XP_006724899.1:p.Ala117Ser
XM_006724837.1:c.349G>T	XP_006724900.1:p.Ala117Ser
XM_006724839.1:c.349G>T	XP_006724902.1:p.Ala117Ser
XM_006724841.2:c.88G>T	XP_006724904.1:p.Ala30Ser
XM_006724842.2:c.88G>T	XP_006724905.1:p.Ala30Ser
XM_011531189.1:c.349G>T	XP_011529491.1:p.Ala117Ser
XM_011531190.1:c.88G>T	XP_011529492.1:p.Ala30Ser
XM_011531191.1:c.19G>T	XP_011529493.1:p.Ala7Ser
XM_011531192.1:c.16G>T	XP_011529494.1:p.Ala6Ser
XR_938511.1:n.652G>T
XM_006724841.4:c.88G>T	XP_006724904.1:p.Ala30Ser
XM_006724842.4:c.88G>T	XP_006724905.1:p.Ala30Ser
XM_011531191.2:c.19G>T	XP_011529493.1:p.Ala7Ser
XM_017029761.1:c.295G>T	XP_016885250.1:p.Ala99Ser
XM_017029762.1:c.349G>T	XP_016885251.1:p.Ala117Ser
XM_017029763.1:c.295G>T	XP_016885252.1:p.Ala99Ser
XM_017029764.1:c.16G>T	XP_016885253.1:p.Ala6Ser
XM_017029765.2:c.88G>T	XP_016885254.1:p.Ala30Ser
XM_024452431.1:c.349G>T	XP_024308199.1:p.Ala117Ser
NM_000116.5:c.295G>T MANE Select	NP_000107.1:p.Ala99Ser
NM_001303465.2:c.349G>T	NP_001290394.1:p.Ala117Ser
NM_181311.4:c.295G>T	NP_851828.1:p.Ala99Ser
NM_181312.4:c.295G>T	NP_851829.1:p.Ala99Ser
NM_181313.4:c.295G>T	NP_851830.1:p.Ala99Ser
NR_024048.3:n.706G>T