Canonical Allele Identifier: CA415180693
Gene: TAFAZZIN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154413239A>G , CM000685.2:g.154413239A>G GRCh38
NC_000023.10:g.153641576A>G , CM000685.1:g.153641576A>G GRCh37
NC_000023.9:g.153294770A>G NCBI36
NG_009634.1:g.6700A>G
NG_012884.2:g.3850T>C
NG_009634.2:g.6705A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698234.1:n.699A>G
ENST00000698235.1:n.258A>G
ENST00000698317.1:n.1225A>G
ENST00000698318.1:n.1086A>G
ENST00000470127.2:n.320A>G
ENST00000475699.6:c.325A>G ENSP00000419854.3:p.Lys109Glu
ENST00000476800.2:n.1228A>G
ENST00000483674.3:n.162A>G
ENST00000601016.6:c.271A>G MANE Select ENSP00000469981.1:p.Lys91Glu
ENST00000612012.5:c.271A>G ENSP00000482070.2:p.Lys91Glu
ENST00000612460.5:c.271A>G ENSP00000481037.1:p.Lys91Glu
ENST00000614595.2:n.1621A>G
ENST00000615658.5:n.584A>G
ENST00000616020.5:c.325A>G ENSP00000483636.2:p.Lys109Glu
ENST00000617701.5:c.271A>G ENSP00000481645.1:p.Lys91Glu
ENST00000621647.2:n.324A>G
ENST00000652354.1:c.-6A>G ENSP00000498734.1:n.-6A>G
ENST00000652358.1:c.-24A>G ENSP00000498464.1:n.-24A>G
ENST00000652390.1:c.190A>G ENSP00000498858.1:p.Lys64Glu
ENST00000652476.1:n.432A>G
ENST00000652682.1:c.271A>G ENSP00000498288.1:p.Lys91Glu
ENST00000652685.1:n.323A>G
ENST00000369776.8:c.196A>G ENSP00000358791.4:p.Lys66Glu
ENST00000426231.5:c.87A>G
ENST00000439735.2:c.271A>G ENSP00000398193.1:p.Lys91Glu
ENST00000475699.5:c.271A>G ENSP00000419854.2:p.Lys91Glu
ENST00000476679.5:n.184A>G
ENST00000476800.1:n.149A>G
ENST00000479875.1:n.300A>G
ENST00000483780.5:n.45A>G
ENST00000601016.5:c.271A>G ENSP00000469981.1:p.Lys91Glu
ENST00000612012.4:c.325A>G ENSP00000482070.1:p.Lys109Glu
ENST00000612460.4:c.271A>G ENSP00000481037.1:p.Lys91Glu
ENST00000613002.4:c.271A>G ENSP00000478154.1:p.Lys91Glu
ENST00000613634.4:n.591A>G
ENST00000615658.4:n.597A>G
ENST00000615986.4:c.271A>G ENSP00000480133.1:p.Lys91Glu
ENST00000616020.4:c.325A>G ENSP00000483636.1:p.Lys109Glu
ENST00000617701.4:c.271A>G ENSP00000481645.1:p.Lys91Glu
ENST00000620808.4:c.271A>G ENSP00000479311.1:p.Lys91Glu
ENST00000621647.1:n.556A>G
NM_000116.4:c.271A>G NP_000107.1:p.Lys91Glu
NM_001303465.1:c.325A>G NP_001290394.1:p.Lys109Glu
NM_181311.3:c.271A>G NP_851828.1:p.Lys91Glu
NM_181312.3:c.271A>G NP_851829.1:p.Lys91Glu
NM_181313.3:c.271A>G NP_851830.1:p.Lys91Glu
NR_024048.2:n.597A>G
XM_006724836.1:c.325A>G XP_006724899.1:p.Lys109Glu
XM_006724837.1:c.325A>G XP_006724900.1:p.Lys109Glu
XM_006724839.1:c.325A>G XP_006724902.1:p.Lys109Glu
XM_006724841.2:c.-24A>G XP_006724904.1:n.-24A>G
XM_006724842.2:c.-24A>G XP_006724905.1:n.-24A>G
XM_011531189.1:c.325A>G XP_011529491.1:p.Lys109Glu
XM_011531190.1:c.-24A>G XP_011529492.1:n.-24A>G
XM_011531191.1:c.-6A>G XP_011529493.1:n.-6A>G
XM_011531192.1:c.-127A>G XP_011529494.1:n.-127A>G
XR_938511.1:n.628A>G
XM_006724841.4:c.-24A>G XP_006724904.1:n.-24A>G
XM_006724842.4:c.-24A>G XP_006724905.1:n.-24A>G
XM_011531191.2:c.-6A>G XP_011529493.1:n.-6A>G
XM_017029761.1:c.271A>G XP_016885250.1:p.Lys91Glu
XM_017029762.1:c.325A>G XP_016885251.1:p.Lys109Glu
XM_017029763.1:c.271A>G XP_016885252.1:p.Lys91Glu
XM_017029764.1:c.-127A>G XP_016885253.1:n.-127A>G
XM_017029765.2:c.-24A>G XP_016885254.1:n.-24A>G
XM_024452431.1:c.325A>G XP_024308199.1:p.Lys109Glu
NM_000116.5:c.271A>G MANE Select NP_000107.1:p.Lys91Glu
NM_001303465.2:c.325A>G NP_001290394.1:p.Lys109Glu
NM_181311.4:c.271A>G NP_851828.1:p.Lys91Glu
NM_181312.4:c.271A>G NP_851829.1:p.Lys91Glu
NM_181313.4:c.271A>G NP_851830.1:p.Lys91Glu
NR_024048.3:n.576A>G