Canonical Allele Identifier: CA2466677625
Gene: TAFAZZIN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154420234C= , CM000685.2:g.154420234C= GRCh38
NC_000023.10:g.153648573C= , CM000685.1:g.153648573C= GRCh37
NC_000023.9:g.153301767C= NCBI36
NG_009634.1:g.13697C=
NG_009634.2:g.13700C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.1479C=
ENST00000698317.1:n.2095C=
ENST00000698318.1:n.1878C=
ENST00000698319.1:n.1241C=
ENST00000698320.1:n.1129C=
ENST00000470127.2:n.1142C=
ENST00000475699.6:c.633C= ENSP00000419854.3:p.Asn211=
ENST00000483674.3:n.551C=
ENST00000601016.6:c.669C= MANE Select ENSP00000469981.1:p.Asn223=
ENST00000612012.5:c.627C= ENSP00000482070.2:p.Asn209=
ENST00000612460.5:c.579C= ENSP00000481037.1:p.Asn193=
ENST00000614595.2:n.2016C=
ENST00000615658.5:n.1258C=
ENST00000616020.5:c.681C= ENSP00000483636.2:p.Asn227=
ENST00000617701.5:c.*682C= ENSP00000481645.1:n.*682C=
ENST00000652354.1:c.351C= ENSP00000498734.1:p.Asn117=
ENST00000652358.1:c.462C= ENSP00000498464.1:p.Asn154=
ENST00000652390.1:c.588C= ENSP00000498858.1:p.Asn196=
ENST00000652476.1:n.1335C=
ENST00000652644.1:c.282C= ENSP00000498496.1:p.Asn94=
ENST00000652682.1:c.726C= ENSP00000498288.1:p.Asn242=
ENST00000652685.1:n.1022C=
ENST00000369776.8:c.579C= ENSP00000358791.4:p.Asn193=
ENST00000426231.5:c.666C=
ENST00000475699.5:c.627C= ENSP00000419854.2:p.Asn209=
ENST00000494912.5:n.1358C=
ENST00000498029.1:n.127C=
ENST00000601016.5:c.669C= ENSP00000469981.1:p.Asn223=
ENST00000612460.4:c.579C= ENSP00000481037.1:p.Asn193=
ENST00000613002.4:c.537C= ENSP00000478154.1:p.Asn179=
ENST00000615986.4:c.*397C= ENSP00000480133.1:n.*397C=
NM_000116.4:c.669C= NP_000107.1:p.Asn223=
NM_001303465.1:c.681C= NP_001290394.1:p.Asn227=
NM_181311.3:c.579C= NP_851828.1:p.Asn193=
NM_181312.3:c.627C= NP_851829.1:p.Asn209=
NM_181313.3:c.537C= NP_851830.1:p.Asn179=
NR_024048.2:n.1011C=
XM_006724836.1:c.723C= XP_006724899.1:p.Asn241=
XM_006724837.1:c.708C= XP_006724900.1:p.Asn236=
XM_006724839.1:c.591C= XP_006724902.1:p.Asn197=
XM_006724841.2:c.462C= XP_006724904.1:p.Asn154=
XM_006724842.2:c.372C= XP_006724905.1:p.Asn124=
XM_011531189.1:c.510C= XP_011529491.1:p.Asn170=
XM_011531190.1:c.462C= XP_011529492.1:p.Asn154=
XM_011531191.1:c.393C= XP_011529493.1:p.Asn131=
XM_011531192.1:c.390C= XP_011529494.1:p.Asn130=
XR_938511.1:n.1017C=
XM_006724841.4:c.462C= XP_006724904.1:p.Asn154=
XM_006724842.4:c.372C= XP_006724905.1:p.Asn124=
XM_011531191.2:c.393C= XP_011529493.1:p.Asn131=
XM_017029761.1:c.654C= XP_016885250.1:p.Asn218=
XM_017029762.1:c.633C= XP_016885251.1:p.Asn211=
XM_017029763.1:c.456C= XP_016885252.1:p.Asn152=
XM_017029764.1:c.390C= XP_016885253.1:p.Asn130=
XM_017029765.2:c.330C= XP_016885254.1:p.Asn110=
XM_024452431.1:c.627C= XP_024308199.1:p.Asn209=
NM_000116.5:c.669C= MANE Select NP_000107.1:p.Asn223=
NM_001303465.2:c.681C= NP_001290394.1:p.Asn227=
NM_181311.4:c.579C= NP_851828.1:p.Asn193=
NM_181312.4:c.627C= NP_851829.1:p.Asn209=
NM_181313.4:c.537C= NP_851830.1:p.Asn179=
NR_024048.3:n.990C=