Canonical Allele Identifier: CA415179644

Gene: TAFAZZIN

Linked Data

• ClinVar Variation Id: 2112174
• ClinVar RCV Id: RCV003034414
• MyVariant Identifiers: chrX:g.153640466C>A (hg19) ; chrX:g.154412129C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154412129C>A , CM000685.2:g.154412129C>A	GRCh38
NC_000023.10:g.153640466C>A , CM000685.1:g.153640466C>A	GRCh37
NC_000023.9:g.153293660C>A	NCBI36
NG_009634.1:g.5590C>A
NG_012884.2:g.4960G>T
NG_009634.2:g.5595C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.581C>A
ENST00000698235.1:n.140C>A
ENST00000698317.1:n.115C>A
ENST00000475699.6:c.207C>A	ENSP00000419854.3:p.Tyr69Ter
ENST00000476800.2:n.118C>A
ENST00000483674.3:n.44C>A
ENST00000601016.6:c.153C>A MANE Select	ENSP00000469981.1:p.Tyr51Ter
ENST00000612012.5:c.153C>A	ENSP00000482070.2:p.Tyr51Ter
ENST00000612460.5:c.153C>A	ENSP00000481037.1:p.Tyr51Ter
ENST00000614595.2:n.511C>A
ENST00000615658.5:n.466C>A
ENST00000616020.5:c.207C>A	ENSP00000483636.2:p.Tyr69Ter
ENST00000617701.5:c.153C>A	ENSP00000481645.1:p.Tyr51Ter
ENST00000621647.2:n.206C>A
ENST00000652358.1:c.-57+177C>A	ENSP00000498464.1:n.-57+177C>A
ENST00000652390.1:c.72C>A	ENSP00000498858.1:p.Tyr24Ter
ENST00000652476.1:n.314C>A
ENST00000652682.1:c.153C>A	ENSP00000498288.1:p.Tyr51Ter
ENST00000652685.1:n.205C>A
ENST00000369776.8:c.163+123C>A	ENSP00000358791.4:n.163+123C>A
ENST00000439735.2:c.153C>A	ENSP00000398193.1:p.Tyr51Ter
ENST00000475699.5:c.153C>A	ENSP00000419854.2:p.Tyr51Ter
ENST00000601016.5:c.153C>A	ENSP00000469981.1:p.Tyr51Ter
ENST00000612012.4:c.207C>A	ENSP00000482070.1:p.Tyr69Ter
ENST00000612460.4:c.153C>A	ENSP00000481037.1:p.Tyr51Ter
ENST00000613002.4:c.153C>A	ENSP00000478154.1:p.Tyr51Ter
ENST00000613634.4:n.473C>A
ENST00000614595.1:n.372C>A
ENST00000615658.4:n.479C>A
ENST00000615986.4:c.153C>A	ENSP00000480133.1:p.Tyr51Ter
ENST00000616020.4:c.207C>A	ENSP00000483636.1:p.Tyr69Ter
ENST00000617701.4:c.153C>A	ENSP00000481645.1:p.Tyr51Ter
ENST00000620808.4:c.153C>A	ENSP00000479311.1:p.Tyr51Ter
ENST00000621647.1:n.438C>A
NM_000116.4:c.153C>A	NP_000107.1:p.Tyr51Ter
NM_001303465.1:c.207C>A	NP_001290394.1:p.Tyr69Ter
NM_181311.3:c.153C>A	NP_851828.1:p.Tyr51Ter
NM_181312.3:c.153C>A	NP_851829.1:p.Tyr51Ter
NM_181313.3:c.153C>A	NP_851830.1:p.Tyr51Ter
NR_024048.2:n.479C>A
XM_006724836.1:c.207C>A	XP_006724899.1:p.Tyr69Ter
XM_006724837.1:c.207C>A	XP_006724900.1:p.Tyr69Ter
XM_006724839.1:c.207C>A	XP_006724902.1:p.Tyr69Ter
XM_006724841.2:c.-142C>A	XP_006724904.1:n.-142C>A
XM_006724842.2:c.-142C>A	XP_006724905.1:n.-142C>A
XM_011531189.1:c.207C>A	XP_011529491.1:p.Tyr69Ter
XR_938511.1:n.510C>A
XM_006724841.4:c.-142C>A	XP_006724904.1:n.-142C>A
XM_006724842.4:c.-142C>A	XP_006724905.1:n.-142C>A
XM_017029761.1:c.153C>A	XP_016885250.1:p.Tyr51Ter
XM_017029762.1:c.207C>A	XP_016885251.1:p.Tyr69Ter
XM_017029763.1:c.153C>A	XP_016885252.1:p.Tyr51Ter
XM_017029765.2:c.-142C>A	XP_016885254.1:n.-142C>A
XM_024452431.1:c.207C>A	XP_024308199.1:p.Tyr69Ter
NM_000116.5:c.153C>A MANE Select	NP_000107.1:p.Tyr51Ter
NM_001303465.2:c.207C>A	NP_001290394.1:p.Tyr69Ter
NM_181311.4:c.153C>A	NP_851828.1:p.Tyr51Ter
NM_181312.4:c.153C>A	NP_851829.1:p.Tyr51Ter
NM_181313.4:c.153C>A	NP_851830.1:p.Tyr51Ter
NR_024048.3:n.458C>A