Canonical Allele Identifier: CA873319188

Gene: TAFAZZIN

Linked Data

• dbSNP Id: rs1251768200
• MyVariant Identifiers: chrX:g.154420544_154420545insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154420548dup , CM000685.2:g.154420548dup	GRCh38
NC_000023.10:g.153648887dup , CM000685.1:g.153648887dup	GRCh37
NC_000023.9:g.153302081dup	NCBI36
NG_009634.1:g.14011dup
NG_009634.2:g.14014dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.1510-110dup
ENST00000698317.1:n.2126-110dup
ENST00000698318.1:n.1909-110dup
ENST00000698319.1:n.1272-110dup
ENST00000698320.1:n.1160-110dup
ENST00000470127.2:n.1173-110dup
ENST00000475699.6:c.664-110dup	ENSP00000419854.3:n.664-110dup
ENST00000483674.3:n.582-110dup
ENST00000601016.6:c.700-110dup MANE Select	ENSP00000469981.1:n.700-110dup
ENST00000612012.5:c.658-110dup	ENSP00000482070.2:n.658-110dup
ENST00000612460.5:c.610-110dup	ENSP00000481037.1:n.610-110dup
ENST00000614595.2:n.2047-110dup
ENST00000615658.5:n.1289-110dup
ENST00000616020.5:c.712-110dup	ENSP00000483636.2:n.712-110dup
ENST00000617701.5:c.*713-110dup	ENSP00000481645.1:n.*713-110dup
ENST00000651139.1:c.-85+89dup	ENSP00000498957.1:n.-85+89dup
ENST00000652354.1:c.382-110dup	ENSP00000498734.1:n.382-110dup
ENST00000652358.1:c.493-110dup	ENSP00000498464.1:n.493-110dup
ENST00000652390.1:c.619-110dup	ENSP00000498858.1:n.619-110dup
ENST00000652476.1:n.1366-110dup
ENST00000652644.1:c.313-110dup	ENSP00000498496.1:n.313-110dup
ENST00000652682.1:c.757-110dup	ENSP00000498288.1:n.757-110dup
ENST00000652685.1:n.1053-110dup
ENST00000369776.8:c.610-110dup	ENSP00000358791.4:n.610-110dup
ENST00000426231.5:c.697-110dup
ENST00000475699.5:c.658-110dup	ENSP00000419854.2:n.658-110dup
ENST00000494912.5:n.1389-110dup
ENST00000498029.1:n.158-110dup
ENST00000601016.5:c.700-110dup	ENSP00000469981.1:n.700-110dup
ENST00000612460.4:c.610-110dup	ENSP00000481037.1:n.610-110dup
ENST00000613002.4:c.568-110dup	ENSP00000478154.1:n.568-110dup
ENST00000615986.4:c.*428-110dup	ENSP00000480133.1:n.*428-110dup
NM_000116.4:c.700-110dup	NP_000107.1:n.700-110dup
NM_001303465.1:c.712-110dup	NP_001290394.1:n.712-110dup
NM_181311.3:c.610-110dup	NP_851828.1:n.610-110dup
NM_181312.3:c.658-110dup	NP_851829.1:n.658-110dup
NM_181313.3:c.568-110dup	NP_851830.1:n.568-110dup
NR_024048.2:n.1042-110dup
XM_006724836.1:c.754-110dup	XP_006724899.1:n.754-110dup
XM_006724837.1:c.739-110dup	XP_006724900.1:n.739-110dup
XM_006724839.1:c.622-110dup	XP_006724902.1:n.622-110dup
XM_006724841.2:c.493-110dup	XP_006724904.1:n.493-110dup
XM_006724842.2:c.403-110dup	XP_006724905.1:n.403-110dup
XM_011531189.1:c.541-110dup	XP_011529491.1:n.541-110dup
XM_011531190.1:c.493-110dup	XP_011529492.1:n.493-110dup
XM_011531191.1:c.424-110dup	XP_011529493.1:n.424-110dup
XM_011531192.1:c.421-110dup	XP_011529494.1:n.421-110dup
XR_938511.1:n.1048-110dup
XM_006724841.4:c.493-110dup	XP_006724904.1:n.493-110dup
XM_006724842.4:c.403-110dup	XP_006724905.1:n.403-110dup
XM_011531191.2:c.424-110dup	XP_011529493.1:n.424-110dup
XM_017029761.1:c.685-110dup	XP_016885250.1:n.685-110dup
XM_017029762.1:c.664-110dup	XP_016885251.1:n.664-110dup
XM_017029763.1:c.487-110dup	XP_016885252.1:n.487-110dup
XM_017029764.1:c.421-110dup	XP_016885253.1:n.421-110dup
XM_017029765.2:c.361-110dup	XP_016885254.1:n.361-110dup
XM_024452431.1:c.658-110dup	XP_024308199.1:n.658-110dup
NM_000116.5:c.700-110dup MANE Select	NP_000107.1:n.700-110dup
NM_001303465.2:c.712-110dup	NP_001290394.1:n.712-110dup
NM_181311.4:c.610-110dup	NP_851828.1:n.610-110dup
NM_181312.4:c.658-110dup	NP_851829.1:n.658-110dup
NM_181313.4:c.568-110dup	NP_851830.1:n.568-110dup
NR_024048.3:n.1021-110dup