Canonical Allele Identifier: CA2466677826

Gene: TAFAZZIN

Linked Data

• dbSNP Id: rs2068608861

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420781C>T , CM000685.2:g.154420781C>T	GRCh38
NC_000023.10:g.153649120C>T , CM000685.1:g.153649120C>T	GRCh37
NC_000023.9:g.153302314C>T	NCBI36
NG_009634.1:g.14244C>T
NG_009634.2:g.14247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1587+46C>T
ENST00000698317.1:n.2203+46C>T
ENST00000698318.1:n.1986+46C>T
ENST00000698319.1:n.1349+46C>T
ENST00000698320.1:n.1283C>T
ENST00000470127.2:n.1250+46C>T
ENST00000475699.6:c.741+46C>T	ENSP00000419854.3:n.741+46C>T
ENST00000483674.3:n.659+46C>T
ENST00000601016.6:c.777+46C>T MANE Select	ENSP00000469981.1:n.777+46C>T
ENST00000612012.5:c.735+46C>T	ENSP00000482070.2:n.735+46C>T
ENST00000612460.5:c.687+46C>T	ENSP00000481037.1:n.687+46C>T
ENST00000614595.2:n.2124+46C>T
ENST00000615658.5:n.1366+46C>T
ENST00000616020.5:c.789+46C>T	ENSP00000483636.2:n.789+46C>T
ENST00000617701.5:c.*790+46C>T	ENSP00000481645.1:n.*790+46C>T
ENST00000651139.1:c.-7+46C>T	ENSP00000498957.1:n.-7+46C>T
ENST00000652354.1:c.459+46C>T	ENSP00000498734.1:n.459+46C>T
ENST00000652358.1:c.570+46C>T	ENSP00000498464.1:n.570+46C>T
ENST00000652390.1:c.696+46C>T	ENSP00000498858.1:n.696+46C>T
ENST00000652476.1:n.1443+46C>T
ENST00000652644.1:c.390+46C>T	ENSP00000498496.1:n.390+46C>T
ENST00000652682.1:c.834+46C>T	ENSP00000498288.1:n.834+46C>T
ENST00000652685.1:n.1130+46C>T
ENST00000369776.8:c.687+46C>T	ENSP00000358791.4:n.687+46C>T
ENST00000426231.5:c.774+46C>T
ENST00000475699.5:c.735+46C>T	ENSP00000419854.2:n.735+46C>T
ENST00000494912.5:n.1466+46C>T
ENST00000498029.1:n.235+46C>T
ENST00000601016.5:c.777+46C>T	ENSP00000469981.1:n.777+46C>T
ENST00000612460.4:c.687+46C>T	ENSP00000481037.1:n.687+46C>T
ENST00000613002.4:c.645+46C>T	ENSP00000478154.1:n.645+46C>T
ENST00000615986.4:c.*505+46C>T	ENSP00000480133.1:n.*505+46C>T
NM_000116.4:c.777+46C>T	NP_000107.1:n.777+46C>T
NM_001303465.1:c.789+46C>T	NP_001290394.1:n.789+46C>T
NM_181311.3:c.687+46C>T	NP_851828.1:n.687+46C>T
NM_181312.3:c.735+46C>T	NP_851829.1:n.735+46C>T
NM_181313.3:c.645+46C>T	NP_851830.1:n.645+46C>T
NR_024048.2:n.1119+46C>T
XM_006724836.1:c.831+46C>T	XP_006724899.1:n.831+46C>T
XM_006724837.1:c.816+46C>T	XP_006724900.1:n.816+46C>T
XM_006724839.1:c.699+46C>T	XP_006724902.1:n.699+46C>T
XM_006724841.2:c.570+46C>T	XP_006724904.1:n.570+46C>T
XM_006724842.2:c.480+46C>T	XP_006724905.1:n.480+46C>T
XM_011531189.1:c.618+46C>T	XP_011529491.1:n.618+46C>T
XM_011531190.1:c.570+46C>T	XP_011529492.1:n.570+46C>T
XM_011531191.1:c.501+46C>T	XP_011529493.1:n.501+46C>T
XM_011531192.1:c.498+46C>T	XP_011529494.1:n.498+46C>T
XR_938511.1:n.1125+46C>T
XM_006724841.4:c.570+46C>T	XP_006724904.1:n.570+46C>T
XM_006724842.4:c.480+46C>T	XP_006724905.1:n.480+46C>T
XM_011531191.2:c.501+46C>T	XP_011529493.1:n.501+46C>T
XM_017029761.1:c.762+46C>T	XP_016885250.1:n.762+46C>T
XM_017029762.1:c.741+46C>T	XP_016885251.1:n.741+46C>T
XM_017029763.1:c.564+46C>T	XP_016885252.1:n.564+46C>T
XM_017029764.1:c.498+46C>T	XP_016885253.1:n.498+46C>T
XM_017029765.2:c.438+46C>T	XP_016885254.1:n.438+46C>T
XM_024452431.1:c.735+46C>T	XP_024308199.1:n.735+46C>T
NM_000116.5:c.777+46C>T MANE Select	NP_000107.1:n.777+46C>T
NM_001303465.2:c.789+46C>T	NP_001290394.1:n.789+46C>T
NM_181311.4:c.687+46C>T	NP_851828.1:n.687+46C>T
NM_181312.4:c.735+46C>T	NP_851829.1:n.735+46C>T
NM_181313.4:c.645+46C>T	NP_851830.1:n.645+46C>T
NR_024048.3:n.1098+46C>T