Canonical Allele Identifier: CA10577661

Gene: TAFAZZIN

Linked Data

• ClinVar Variation Id: 234603
• ClinVar RCV Id: RCV000216377 ; RCV003236792
• dbSNP Id: rs876661112
• MyVariant Identifiers: chrX:g.153649240A>G (hg19) ; chrX:g.154420901A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420901A>G , CM000685.2:g.154420901A>G	GRCh38
NC_000023.10:g.153649240A>G , CM000685.1:g.153649240A>G	GRCh37
NC_000023.9:g.153302434A>G	NCBI36
NG_009634.1:g.14364A>G
NG_009634.2:g.14367A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1588-2A>G
ENST00000698317.1:n.2204-2A>G
ENST00000698318.1:n.1987-2A>G
ENST00000698319.1:n.1350-2A>G
ENST00000698320.1:n.1403A>G
ENST00000470127.2:n.1251-2A>G
ENST00000475699.6:c.742-2A>G	ENSP00000419854.3:n.742-2A>G
ENST00000483674.3:n.660-2A>G
ENST00000601016.6:c.778-2A>G MANE Select	ENSP00000469981.1:n.778-2A>G
ENST00000612012.5:c.736-2A>G	ENSP00000482070.2:n.736-2A>G
ENST00000612460.5:c.688-2A>G	ENSP00000481037.1:n.688-2A>G
ENST00000614595.2:n.2125-2A>G
ENST00000615658.5:n.1367-2A>G
ENST00000616020.5:c.790-2A>G	ENSP00000483636.2:n.790-2A>G
ENST00000617701.5:c.*791-2A>G	ENSP00000481645.1:n.*791-2A>G
ENST00000651139.1:c.-6-2A>G	ENSP00000498957.1:n.-6-2A>G
ENST00000652354.1:c.460-2A>G	ENSP00000498734.1:n.460-2A>G
ENST00000652358.1:c.571-2A>G	ENSP00000498464.1:n.571-2A>G
ENST00000652390.1:c.697-2A>G	ENSP00000498858.1:n.697-2A>G
ENST00000652476.1:n.1444-2A>G
ENST00000652644.1:c.391-2A>G	ENSP00000498496.1:n.391-2A>G
ENST00000652682.1:c.835-2A>G	ENSP00000498288.1:n.835-2A>G
ENST00000652685.1:n.1131-2A>G
ENST00000369776.8:c.688-2A>G	ENSP00000358791.4:n.688-2A>G
ENST00000426231.5:c.775-2A>G
ENST00000475699.5:c.736-2A>G	ENSP00000419854.2:n.736-2A>G
ENST00000494912.5:n.1467-2A>G
ENST00000498029.1:n.236-2A>G
ENST00000601016.5:c.778-2A>G	ENSP00000469981.1:n.778-2A>G
ENST00000612460.4:c.688-2A>G	ENSP00000481037.1:n.688-2A>G
ENST00000613002.4:c.646-2A>G	ENSP00000478154.1:n.646-2A>G
ENST00000615986.4:c.*506-2A>G	ENSP00000480133.1:n.*506-2A>G
NM_000116.4:c.778-2A>G	NP_000107.1:n.778-2A>G
NM_001303465.1:c.790-2A>G	NP_001290394.1:n.790-2A>G
NM_181311.3:c.688-2A>G	NP_851828.1:n.688-2A>G
NM_181312.3:c.736-2A>G	NP_851829.1:n.736-2A>G
NM_181313.3:c.646-2A>G	NP_851830.1:n.646-2A>G
NR_024048.2:n.1120-2A>G
XM_006724836.1:c.832-2A>G	XP_006724899.1:n.832-2A>G
XM_006724837.1:c.817-2A>G	XP_006724900.1:n.817-2A>G
XM_006724839.1:c.700-2A>G	XP_006724902.1:n.700-2A>G
XM_006724841.2:c.571-2A>G	XP_006724904.1:n.571-2A>G
XM_006724842.2:c.481-2A>G	XP_006724905.1:n.481-2A>G
XM_011531189.1:c.619-2A>G	XP_011529491.1:n.619-2A>G
XM_011531190.1:c.571-2A>G	XP_011529492.1:n.571-2A>G
XM_011531191.1:c.502-2A>G	XP_011529493.1:n.502-2A>G
XM_011531192.1:c.499-2A>G	XP_011529494.1:n.499-2A>G
XR_938511.1:n.1126-2A>G
XM_006724841.4:c.571-2A>G	XP_006724904.1:n.571-2A>G
XM_006724842.4:c.481-2A>G	XP_006724905.1:n.481-2A>G
XM_011531191.2:c.502-2A>G	XP_011529493.1:n.502-2A>G
XM_017029761.1:c.763-2A>G	XP_016885250.1:n.763-2A>G
XM_017029762.1:c.742-2A>G	XP_016885251.1:n.742-2A>G
XM_017029763.1:c.565-2A>G	XP_016885252.1:n.565-2A>G
XM_017029764.1:c.499-2A>G	XP_016885253.1:n.499-2A>G
XM_017029765.2:c.439-2A>G	XP_016885254.1:n.439-2A>G
XM_024452431.1:c.736-2A>G	XP_024308199.1:n.736-2A>G
NM_000116.5:c.778-2A>G MANE Select	NP_000107.1:n.778-2A>G
NM_001303465.2:c.790-2A>G	NP_001290394.1:n.790-2A>G
NM_181311.4:c.688-2A>G	NP_851828.1:n.688-2A>G
NM_181312.4:c.736-2A>G	NP_851829.1:n.736-2A>G
NM_181313.4:c.646-2A>G	NP_851830.1:n.646-2A>G
NR_024048.3:n.1099-2A>G