Canonical Allele Identifier: CA2824301270

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420535A>G , CM000685.2:g.154420535A>G	GRCh38
NC_000023.10:g.153648874A>G , CM000685.1:g.153648874A>G	GRCh37
NC_000023.9:g.153302068A>G	NCBI36
NG_009634.1:g.13998A>G
NG_009634.2:g.14001A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.1510-123A>G
ENST00000698317.1:n.2126-123A>G
ENST00000698318.1:n.1909-123A>G
ENST00000698319.1:n.1272-123A>G
ENST00000698320.1:n.1160-123A>G
ENST00000470127.2:n.1173-123A>G
ENST00000475699.6:c.664-123A>G	ENSP00000419854.3:n.664-123A>G
ENST00000483674.3:n.582-123A>G
ENST00000601016.6:c.700-123A>G MANE Select	ENSP00000469981.1:n.700-123A>G
ENST00000612012.5:c.658-123A>G	ENSP00000482070.2:n.658-123A>G
ENST00000612460.5:c.610-123A>G	ENSP00000481037.1:n.610-123A>G
ENST00000614595.2:n.2047-123A>G
ENST00000615658.5:n.1289-123A>G
ENST00000616020.5:c.712-123A>G	ENSP00000483636.2:n.712-123A>G
ENST00000617701.5:c.*713-123A>G	ENSP00000481645.1:n.*713-123A>G
ENST00000651139.1:c.-85+76A>G	ENSP00000498957.1:n.-85+76A>G
ENST00000652354.1:c.382-123A>G	ENSP00000498734.1:n.382-123A>G
ENST00000652358.1:c.493-123A>G	ENSP00000498464.1:n.493-123A>G
ENST00000652390.1:c.619-123A>G	ENSP00000498858.1:n.619-123A>G
ENST00000652476.1:n.1366-123A>G
ENST00000652644.1:c.313-123A>G	ENSP00000498496.1:n.313-123A>G
ENST00000652682.1:c.757-123A>G	ENSP00000498288.1:n.757-123A>G
ENST00000652685.1:n.1053-123A>G
ENST00000369776.8:c.610-123A>G	ENSP00000358791.4:n.610-123A>G
ENST00000426231.5:c.697-123A>G
ENST00000475699.5:c.658-123A>G	ENSP00000419854.2:n.658-123A>G
ENST00000494912.5:n.1389-123A>G
ENST00000498029.1:n.158-123A>G
ENST00000601016.5:c.700-123A>G	ENSP00000469981.1:n.700-123A>G
ENST00000612460.4:c.610-123A>G	ENSP00000481037.1:n.610-123A>G
ENST00000613002.4:c.568-123A>G	ENSP00000478154.1:n.568-123A>G
ENST00000615986.4:c.*428-123A>G	ENSP00000480133.1:n.*428-123A>G
NM_000116.4:c.700-123A>G	NP_000107.1:n.700-123A>G
NM_001303465.1:c.712-123A>G	NP_001290394.1:n.712-123A>G
NM_181311.3:c.610-123A>G	NP_851828.1:n.610-123A>G
NM_181312.3:c.658-123A>G	NP_851829.1:n.658-123A>G
NM_181313.3:c.568-123A>G	NP_851830.1:n.568-123A>G
NR_024048.2:n.1042-123A>G
XM_006724836.1:c.754-123A>G	XP_006724899.1:n.754-123A>G
XM_006724837.1:c.739-123A>G	XP_006724900.1:n.739-123A>G
XM_006724839.1:c.622-123A>G	XP_006724902.1:n.622-123A>G
XM_006724841.2:c.493-123A>G	XP_006724904.1:n.493-123A>G
XM_006724842.2:c.403-123A>G	XP_006724905.1:n.403-123A>G
XM_011531189.1:c.541-123A>G	XP_011529491.1:n.541-123A>G
XM_011531190.1:c.493-123A>G	XP_011529492.1:n.493-123A>G
XM_011531191.1:c.424-123A>G	XP_011529493.1:n.424-123A>G
XM_011531192.1:c.421-123A>G	XP_011529494.1:n.421-123A>G
XR_938511.1:n.1048-123A>G
XM_006724841.4:c.493-123A>G	XP_006724904.1:n.493-123A>G
XM_006724842.4:c.403-123A>G	XP_006724905.1:n.403-123A>G
XM_011531191.2:c.424-123A>G	XP_011529493.1:n.424-123A>G
XM_017029761.1:c.685-123A>G	XP_016885250.1:n.685-123A>G
XM_017029762.1:c.664-123A>G	XP_016885251.1:n.664-123A>G
XM_017029763.1:c.487-123A>G	XP_016885252.1:n.487-123A>G
XM_017029764.1:c.421-123A>G	XP_016885253.1:n.421-123A>G
XM_017029765.2:c.361-123A>G	XP_016885254.1:n.361-123A>G
XM_024452431.1:c.658-123A>G	XP_024308199.1:n.658-123A>G
NM_000116.5:c.700-123A>G MANE Select	NP_000107.1:n.700-123A>G
NM_001303465.2:c.712-123A>G	NP_001290394.1:n.712-123A>G
NM_181311.4:c.610-123A>G	NP_851828.1:n.610-123A>G
NM_181312.4:c.658-123A>G	NP_851829.1:n.658-123A>G
NM_181313.4:c.568-123A>G	NP_851830.1:n.568-123A>G
NR_024048.3:n.1021-123A>G