Canonical Allele Identifier: CA2466677516

Gene: TAFAZZIN

Linked Data

• dbSNP Id: rs2068579753
• gnomAD v4: X-154419894-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154419896del , CM000685.2:g.154419896del	GRCh38
NC_000023.10:g.153648235del , CM000685.1:g.153648235del	GRCh37
NC_000023.9:g.153301429del	NCBI36
NG_009634.1:g.13359del
NG_009634.2:g.13362del

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.1258del
ENST00000698317.1:n.1874del
ENST00000698318.1:n.1657del
ENST00000698319.1:n.1020del
ENST00000698320.1:n.908del
ENST00000470127.2:n.921del
ENST00000475699.6:c.548-136del	ENSP00000419854.3:n.548-136del
ENST00000483674.3:n.466-136del
ENST00000601016.6:c.584-136del MANE Select	ENSP00000469981.1:n.584-136del
ENST00000612012.5:c.542-136del	ENSP00000482070.2:n.542-136del
ENST00000612460.5:c.494-136del	ENSP00000481037.1:n.494-136del
ENST00000614595.2:n.1931-136del
ENST00000615658.5:n.1037del
ENST00000616020.5:c.596-136del	ENSP00000483636.2:n.596-136del
ENST00000617701.5:c.*461del	ENSP00000481645.1:n.*461del
ENST00000652354.1:c.266-136del	ENSP00000498734.1:n.266-136del
ENST00000652358.1:c.377-136del	ENSP00000498464.1:n.377-136del
ENST00000652390.1:c.503-136del	ENSP00000498858.1:n.503-136del
ENST00000652476.1:n.1114del
ENST00000652644.1:c.197-136del	ENSP00000498496.1:n.197-136del
ENST00000652682.1:c.641-136del	ENSP00000498288.1:n.641-136del
ENST00000652685.1:n.801del
ENST00000369776.8:c.377-136del	ENSP00000358791.4:n.377-136del
ENST00000426231.5:c.581-136del
ENST00000439735.2:c.491-136del	ENSP00000398193.1:n.491-136del
ENST00000470127.1:n.163-136del
ENST00000475699.5:c.542-136del	ENSP00000419854.2:n.542-136del
ENST00000476679.5:n.727del
ENST00000494912.5:n.1273-136del
ENST00000601016.5:c.584-136del	ENSP00000469981.1:n.584-136del
ENST00000612012.4:c.548-136del	ENSP00000482070.1:n.548-136del
ENST00000612460.4:c.494-136del	ENSP00000481037.1:n.494-136del
ENST00000613002.4:c.452-136del	ENSP00000478154.1:n.452-136del
ENST00000613634.4:n.963del
ENST00000615658.4:n.1137del
ENST00000615986.4:c.*312-136del	ENSP00000480133.1:n.*312-136del
ENST00000620808.4:c.*170-136del	ENSP00000479311.1:n.*170-136del
NM_000116.4:c.584-136del	NP_000107.1:n.584-136del
NM_001303465.1:c.596-136del	NP_001290394.1:n.596-136del
NM_181311.3:c.494-136del	NP_851828.1:n.494-136del
NM_181312.3:c.542-136del	NP_851829.1:n.542-136del
NM_181313.3:c.452-136del	NP_851830.1:n.452-136del
NR_024048.2:n.926-136del
XM_006724836.1:c.638-136del	XP_006724899.1:n.638-136del
XM_006724837.1:c.506-136del	XP_006724900.1:n.506-136del
XM_006724839.1:c.506-136del	XP_006724902.1:n.506-136del
XM_006724841.2:c.377-136del	XP_006724904.1:n.377-136del
XM_006724842.2:c.287-136del	XP_006724905.1:n.287-136del
XM_011531189.1:c.425-136del	XP_011529491.1:n.425-136del
XM_011531190.1:c.377-136del	XP_011529492.1:n.377-136del
XM_011531191.1:c.308-136del	XP_011529493.1:n.308-136del
XM_011531192.1:c.305-136del	XP_011529494.1:n.305-136del
XR_938511.1:n.932-136del
XM_006724841.4:c.377-136del	XP_006724904.1:n.377-136del
XM_006724842.4:c.287-136del	XP_006724905.1:n.287-136del
XM_011531191.2:c.308-136del	XP_011529493.1:n.308-136del
XM_017029761.1:c.452-136del	XP_016885250.1:n.452-136del
XM_017029762.1:c.548-136del	XP_016885251.1:n.548-136del
XM_017029763.1:c.371-136del	XP_016885252.1:n.371-136del
XM_017029764.1:c.305-136del	XP_016885253.1:n.305-136del
XM_017029765.2:c.245-136del	XP_016885254.1:n.245-136del
XM_024452431.1:c.425-136del	XP_024308199.1:n.425-136del
NM_000116.5:c.584-136del MANE Select	NP_000107.1:n.584-136del
NM_001303465.2:c.596-136del	NP_001290394.1:n.596-136del
NM_181311.4:c.494-136del	NP_851828.1:n.494-136del
NM_181312.4:c.542-136del	NP_851829.1:n.542-136del
NM_181313.4:c.452-136del	NP_851830.1:n.452-136del
NR_024048.3:n.905-136del