Canonical Allele Identifier: CA2579739132

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420624C>A , CM000685.2:g.154420624C>A	GRCh38
NC_000023.10:g.153648963C>A , CM000685.1:g.153648963C>A	GRCh37
NC_000023.9:g.153302157C>A	NCBI36
NG_009634.1:g.14087C>A
NG_009634.2:g.14090C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698234.1:n.1510-34C>A
ENST00000698317.1:n.2126-34C>A
ENST00000698318.1:n.1909-34C>A
ENST00000698319.1:n.1272-34C>A
ENST00000698320.1:n.1160-34C>A
ENST00000470127.2:n.1173-34C>A
ENST00000475699.6:c.664-34C>A	ENSP00000419854.3:n.664-34C>A
ENST00000483674.3:n.582-34C>A
ENST00000601016.6:c.700-34C>A MANE Select	ENSP00000469981.1:n.700-34C>A
ENST00000612012.5:c.658-34C>A	ENSP00000482070.2:n.658-34C>A
ENST00000612460.5:c.610-34C>A	ENSP00000481037.1:n.610-34C>A
ENST00000614595.2:n.2047-34C>A
ENST00000615658.5:n.1289-34C>A
ENST00000616020.5:c.712-34C>A	ENSP00000483636.2:n.712-34C>A
ENST00000617701.5:c.*713-34C>A	ENSP00000481645.1:n.*713-34C>A
ENST00000651139.1:c.-84-34C>A	ENSP00000498957.1:n.-84-34C>A
ENST00000652354.1:c.382-34C>A	ENSP00000498734.1:n.382-34C>A
ENST00000652358.1:c.493-34C>A	ENSP00000498464.1:n.493-34C>A
ENST00000652390.1:c.619-34C>A	ENSP00000498858.1:n.619-34C>A
ENST00000652476.1:n.1366-34C>A
ENST00000652644.1:c.313-34C>A	ENSP00000498496.1:n.313-34C>A
ENST00000652682.1:c.757-34C>A	ENSP00000498288.1:n.757-34C>A
ENST00000652685.1:n.1053-34C>A
ENST00000369776.8:c.610-34C>A	ENSP00000358791.4:n.610-34C>A
ENST00000426231.5:c.697-34C>A
ENST00000475699.5:c.658-34C>A	ENSP00000419854.2:n.658-34C>A
ENST00000494912.5:n.1389-34C>A
ENST00000498029.1:n.158-34C>A
ENST00000601016.5:c.700-34C>A	ENSP00000469981.1:n.700-34C>A
ENST00000612460.4:c.610-34C>A	ENSP00000481037.1:n.610-34C>A
ENST00000613002.4:c.568-34C>A	ENSP00000478154.1:n.568-34C>A
ENST00000615986.4:c.*428-34C>A	ENSP00000480133.1:n.*428-34C>A
NM_000116.4:c.700-34C>A	NP_000107.1:n.700-34C>A
NM_001303465.1:c.712-34C>A	NP_001290394.1:n.712-34C>A
NM_181311.3:c.610-34C>A	NP_851828.1:n.610-34C>A
NM_181312.3:c.658-34C>A	NP_851829.1:n.658-34C>A
NM_181313.3:c.568-34C>A	NP_851830.1:n.568-34C>A
NR_024048.2:n.1042-34C>A
XM_006724836.1:c.754-34C>A	XP_006724899.1:n.754-34C>A
XM_006724837.1:c.739-34C>A	XP_006724900.1:n.739-34C>A
XM_006724839.1:c.622-34C>A	XP_006724902.1:n.622-34C>A
XM_006724841.2:c.493-34C>A	XP_006724904.1:n.493-34C>A
XM_006724842.2:c.403-34C>A	XP_006724905.1:n.403-34C>A
XM_011531189.1:c.541-34C>A	XP_011529491.1:n.541-34C>A
XM_011531190.1:c.493-34C>A	XP_011529492.1:n.493-34C>A
XM_011531191.1:c.424-34C>A	XP_011529493.1:n.424-34C>A
XM_011531192.1:c.421-34C>A	XP_011529494.1:n.421-34C>A
XR_938511.1:n.1048-34C>A
XM_006724841.4:c.493-34C>A	XP_006724904.1:n.493-34C>A
XM_006724842.4:c.403-34C>A	XP_006724905.1:n.403-34C>A
XM_011531191.2:c.424-34C>A	XP_011529493.1:n.424-34C>A
XM_017029761.1:c.685-34C>A	XP_016885250.1:n.685-34C>A
XM_017029762.1:c.664-34C>A	XP_016885251.1:n.664-34C>A
XM_017029763.1:c.487-34C>A	XP_016885252.1:n.487-34C>A
XM_017029764.1:c.421-34C>A	XP_016885253.1:n.421-34C>A
XM_017029765.2:c.361-34C>A	XP_016885254.1:n.361-34C>A
XM_024452431.1:c.658-34C>A	XP_024308199.1:n.658-34C>A
NM_000116.5:c.700-34C>A MANE Select	NP_000107.1:n.700-34C>A
NM_001303465.2:c.712-34C>A	NP_001290394.1:n.712-34C>A
NM_181311.4:c.610-34C>A	NP_851828.1:n.610-34C>A
NM_181312.4:c.658-34C>A	NP_851829.1:n.658-34C>A
NM_181313.4:c.568-34C>A	NP_851830.1:n.568-34C>A
NR_024048.3:n.1021-34C>A