Canonical Allele Identifier: CA519277529

Gene: TAFAZZIN

Linked Data

• ClinVar Variation Id: 1148742
• ClinVar RCV Id: RCV001488705
• dbSNP Id: rs2148191873
• MyVariant Identifiers: chrX:g.153641828A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413491A>T , CM000685.2:g.154413491A>T	GRCh38
NC_000023.10:g.153641828A>T , CM000685.1:g.153641828A>T	GRCh37
NC_000023.9:g.153295022A>T	NCBI36
NG_009634.1:g.6952A>T
NG_012884.2:g.3598T>A
NG_009634.2:g.6957A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.828A>T
ENST00000698235.1:n.368A>T
ENST00000698317.1:n.1354A>T
ENST00000698318.1:n.1227A>T
ENST00000470127.2:n.572A>T
ENST00000475699.6:c.348A>T	ENSP00000419854.3:p.Ala116=
ENST00000476800.2:n.1480A>T
ENST00000483674.3:n.185A>T
ENST00000601016.6:c.294A>T MANE Select	ENSP00000469981.1:p.Ala98=
ENST00000612012.5:c.294A>T	ENSP00000482070.2:p.Ala98=
ENST00000612460.5:c.294A>T	ENSP00000481037.1:p.Ala98=
ENST00000614595.2:n.1731A>T
ENST00000615658.5:n.607A>T
ENST00000616020.5:c.348A>T	ENSP00000483636.2:p.Ala116=
ENST00000617701.5:c.*112A>T	ENSP00000481645.1:n.*112A>T
ENST00000621647.2:n.576A>T
ENST00000652354.1:c.18A>T	ENSP00000498734.1:p.Ala6=
ENST00000652358.1:c.87A>T	ENSP00000498464.1:p.Ala29=
ENST00000652390.1:c.213A>T	ENSP00000498858.1:p.Ala71=
ENST00000652476.1:n.684A>T
ENST00000652682.1:c.294A>T	ENSP00000498288.1:p.Ala98=
ENST00000652685.1:n.452A>T
ENST00000369776.8:c.219A>T	ENSP00000358791.4:p.Ala73=
ENST00000426231.5:c.210A>T
ENST00000439735.2:c.294A>T	ENSP00000398193.1:p.Ala98=
ENST00000475699.5:c.294A>T	ENSP00000419854.2:p.Ala98=
ENST00000476679.5:n.207A>T
ENST00000476800.1:n.401A>T
ENST00000479875.1:n.323A>T
ENST00000483674.2:n.3A>T
ENST00000483780.5:n.68A>T
ENST00000601016.5:c.294A>T	ENSP00000469981.1:p.Ala98=
ENST00000612012.4:c.348A>T	ENSP00000482070.1:p.Ala116=
ENST00000612460.4:c.294A>T	ENSP00000481037.1:p.Ala98=
ENST00000613002.4:c.294A>T	ENSP00000478154.1:p.Ala98=
ENST00000613634.4:n.614A>T
ENST00000615658.4:n.707A>T
ENST00000615986.4:c.*112A>T	ENSP00000480133.1:n.*112A>T
ENST00000616020.4:c.348A>T	ENSP00000483636.1:p.Ala116=
ENST00000617701.4:c.*124A>T	ENSP00000481645.1:n.*124A>T
ENST00000620808.4:c.*93A>T	ENSP00000479311.1:n.*93A>T
ENST00000621647.1:n.808A>T
NM_000116.4:c.294A>T	NP_000107.1:p.Ala98=
NM_001303465.1:c.348A>T	NP_001290394.1:p.Ala116=
NM_181311.3:c.294A>T	NP_851828.1:p.Ala98=
NM_181312.3:c.294A>T	NP_851829.1:p.Ala98=
NM_181313.3:c.294A>T	NP_851830.1:p.Ala98=
NR_024048.2:n.726A>T
XM_006724836.1:c.348A>T	XP_006724899.1:p.Ala116=
XM_006724837.1:c.348A>T	XP_006724900.1:p.Ala116=
XM_006724839.1:c.348A>T	XP_006724902.1:p.Ala116=
XM_006724841.2:c.87A>T	XP_006724904.1:p.Ala29=
XM_006724842.2:c.87A>T	XP_006724905.1:p.Ala29=
XM_011531189.1:c.348A>T	XP_011529491.1:p.Ala116=
XM_011531190.1:c.87A>T	XP_011529492.1:p.Ala29=
XM_011531191.1:c.18A>T	XP_011529493.1:p.Ala6=
XM_011531192.1:c.15A>T	XP_011529494.1:p.Ala5=
XR_938511.1:n.651A>T
XM_006724841.4:c.87A>T	XP_006724904.1:p.Ala29=
XM_006724842.4:c.87A>T	XP_006724905.1:p.Ala29=
XM_011531191.2:c.18A>T	XP_011529493.1:p.Ala6=
XM_017029761.1:c.294A>T	XP_016885250.1:p.Ala98=
XM_017029762.1:c.348A>T	XP_016885251.1:p.Ala116=
XM_017029763.1:c.294A>T	XP_016885252.1:p.Ala98=
XM_017029764.1:c.15A>T	XP_016885253.1:p.Ala5=
XM_017029765.2:c.87A>T	XP_016885254.1:p.Ala29=
XM_024452431.1:c.348A>T	XP_024308199.1:p.Ala116=
NM_000116.5:c.294A>T MANE Select	NP_000107.1:p.Ala98=
NM_001303465.2:c.348A>T	NP_001290394.1:p.Ala116=
NM_181311.4:c.294A>T	NP_851828.1:p.Ala98=
NM_181312.4:c.294A>T	NP_851829.1:p.Ala98=
NM_181313.4:c.294A>T	NP_851830.1:p.Ala98=
NR_024048.3:n.705A>T