Canonical Allele Identifier: CA2466677839
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420817T= , CM000685.2:g.154420817T= GRCh38
NC_000023.10:g.153649156T= , CM000685.1:g.153649156T= GRCh37
NC_000023.9:g.153302350T= NCBI36
NG_009634.1:g.14280T=
NG_009634.2:g.14283T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1587+82T=
ENST00000698317.1:n.2203+82T=
ENST00000698318.1:n.1986+82T=
ENST00000698319.1:n.1349+82T=
ENST00000698320.1:n.1319T=
ENST00000470127.2:n.1250+82T=
ENST00000475699.6:c.741+82T= ENSP00000419854.3:n.741+82T=
ENST00000483674.3:n.659+82T=
ENST00000601016.6:c.777+82T= MANE Select ENSP00000469981.1:n.777+82T=
ENST00000612012.5:c.735+82T= ENSP00000482070.2:n.735+82T=
ENST00000612460.5:c.687+82T= ENSP00000481037.1:n.687+82T=
ENST00000614595.2:n.2124+82T=
ENST00000615658.5:n.1366+82T=
ENST00000616020.5:c.789+82T= ENSP00000483636.2:n.789+82T=
ENST00000617701.5:c.*790+82T= ENSP00000481645.1:n.*790+82T=
ENST00000651139.1:c.-7+82T= ENSP00000498957.1:n.-7+82T=
ENST00000652354.1:c.459+82T= ENSP00000498734.1:n.459+82T=
ENST00000652358.1:c.570+82T= ENSP00000498464.1:n.570+82T=
ENST00000652390.1:c.696+82T= ENSP00000498858.1:n.696+82T=
ENST00000652476.1:n.1443+82T=
ENST00000652644.1:c.390+82T= ENSP00000498496.1:n.390+82T=
ENST00000652682.1:c.834+82T= ENSP00000498288.1:n.834+82T=
ENST00000652685.1:n.1130+82T=
ENST00000369776.8:c.687+82T= ENSP00000358791.4:n.687+82T=
ENST00000426231.5:c.774+82T=
ENST00000475699.5:c.735+82T= ENSP00000419854.2:n.735+82T=
ENST00000494912.5:n.1466+82T=
ENST00000498029.1:n.235+82T=
ENST00000601016.5:c.777+82T= ENSP00000469981.1:n.777+82T=
ENST00000612460.4:c.687+82T= ENSP00000481037.1:n.687+82T=
ENST00000613002.4:c.645+82T= ENSP00000478154.1:n.645+82T=
ENST00000615986.4:c.*505+82T= ENSP00000480133.1:n.*505+82T=
NM_000116.4:c.777+82T= NP_000107.1:n.777+82T=
NM_001303465.1:c.789+82T= NP_001290394.1:n.789+82T=
NM_181311.3:c.687+82T= NP_851828.1:n.687+82T=
NM_181312.3:c.735+82T= NP_851829.1:n.735+82T=
NM_181313.3:c.645+82T= NP_851830.1:n.645+82T=
NR_024048.2:n.1119+82T=
XM_006724836.1:c.831+82T= XP_006724899.1:n.831+82T=
XM_006724837.1:c.816+82T= XP_006724900.1:n.816+82T=
XM_006724839.1:c.699+82T= XP_006724902.1:n.699+82T=
XM_006724841.2:c.570+82T= XP_006724904.1:n.570+82T=
XM_006724842.2:c.480+82T= XP_006724905.1:n.480+82T=
XM_011531189.1:c.618+82T= XP_011529491.1:n.618+82T=
XM_011531190.1:c.570+82T= XP_011529492.1:n.570+82T=
XM_011531191.1:c.501+82T= XP_011529493.1:n.501+82T=
XM_011531192.1:c.498+82T= XP_011529494.1:n.498+82T=
XR_938511.1:n.1125+82T=
XM_006724841.4:c.570+82T= XP_006724904.1:n.570+82T=
XM_006724842.4:c.480+82T= XP_006724905.1:n.480+82T=
XM_011531191.2:c.501+82T= XP_011529493.1:n.501+82T=
XM_017029761.1:c.762+82T= XP_016885250.1:n.762+82T=
XM_017029762.1:c.741+82T= XP_016885251.1:n.741+82T=
XM_017029763.1:c.564+82T= XP_016885252.1:n.564+82T=
XM_017029764.1:c.498+82T= XP_016885253.1:n.498+82T=
XM_017029765.2:c.438+82T= XP_016885254.1:n.438+82T=
XM_024452431.1:c.735+82T= XP_024308199.1:n.735+82T=
NM_000116.5:c.777+82T= MANE Select NP_000107.1:n.777+82T=
NM_001303465.2:c.789+82T= NP_001290394.1:n.789+82T=
NM_181311.4:c.687+82T= NP_851828.1:n.687+82T=
NM_181312.4:c.735+82T= NP_851829.1:n.735+82T=
NM_181313.4:c.645+82T= NP_851830.1:n.645+82T=
NR_024048.3:n.1098+82T=