Canonical Allele Identifier: CA2466675180

Gene: TAFAZZIN

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154413031G= , CM000685.2:g.154413031G=	GRCh38
NC_000023.10:g.153641368G= , CM000685.1:g.153641368G=	GRCh37
NC_000023.9:g.153294562G=	NCBI36
NG_009634.1:g.6492G=
NG_012884.2:g.4058C=
NG_009634.2:g.6497G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698234.1:n.667-176G=
ENST00000698235.1:n.226-176G=
ENST00000698317.1:n.1017G=
ENST00000698318.1:n.878G=
ENST00000470127.2:n.112G=
ENST00000475699.6:c.293-176G=	ENSP00000419854.3:n.293-176G=
ENST00000476800.2:n.1020G=
ENST00000483674.3:n.130-176G=
ENST00000601016.6:c.239-176G= MANE Select	ENSP00000469981.1:n.239-176G=
ENST00000612012.5:c.239-176G=	ENSP00000482070.2:n.239-176G=
ENST00000612460.5:c.239-176G=	ENSP00000481037.1:n.239-176G=
ENST00000614595.2:n.1413G=
ENST00000615658.5:n.552-176G=
ENST00000616020.5:c.293-176G=	ENSP00000483636.2:n.293-176G=
ENST00000617701.5:c.239-176G=	ENSP00000481645.1:n.239-176G=
ENST00000621647.2:n.292-176G=
ENST00000652354.1:c.-39+166G=	ENSP00000498734.1:n.-39+166G=
ENST00000652358.1:c.-56-176G=	ENSP00000498464.1:n.-56-176G=
ENST00000652390.1:c.158-176G=	ENSP00000498858.1:n.158-176G=
ENST00000652476.1:n.400-176G=
ENST00000652682.1:c.239-176G=	ENSP00000498288.1:n.239-176G=
ENST00000652685.1:n.291-176G=
ENST00000369776.8:c.164-176G=	ENSP00000358791.4:n.164-176G=
ENST00000426231.5:c.55-176G=
ENST00000439735.2:c.239-176G=	ENSP00000398193.1:n.239-176G=
ENST00000475699.5:c.239-176G=	ENSP00000419854.2:n.239-176G=
ENST00000476679.5:n.151+166G=
ENST00000479875.1:n.267+44G=
ENST00000483780.5:n.13-176G=
ENST00000601016.5:c.239-176G=	ENSP00000469981.1:n.239-176G=
ENST00000612012.4:c.293-176G=	ENSP00000482070.1:n.293-176G=
ENST00000612460.4:c.239-176G=	ENSP00000481037.1:n.239-176G=
ENST00000613002.4:c.239-176G=	ENSP00000478154.1:n.239-176G=
ENST00000613634.4:n.559-176G=
ENST00000615658.4:n.565-176G=
ENST00000615986.4:c.239-176G=	ENSP00000480133.1:n.239-176G=
ENST00000616020.4:c.293-176G=	ENSP00000483636.1:n.293-176G=
ENST00000617701.4:c.239-176G=	ENSP00000481645.1:n.239-176G=
ENST00000620808.4:c.239-176G=	ENSP00000479311.1:n.239-176G=
ENST00000621647.1:n.524-176G=
NM_000116.4:c.239-176G=	NP_000107.1:n.239-176G=
NM_001303465.1:c.293-176G=	NP_001290394.1:n.293-176G=
NM_181311.3:c.239-176G=	NP_851828.1:n.239-176G=
NM_181312.3:c.239-176G=	NP_851829.1:n.239-176G=
NM_181313.3:c.239-176G=	NP_851830.1:n.239-176G=
NR_024048.2:n.565-176G=
XM_006724836.1:c.293-176G=	XP_006724899.1:n.293-176G=
XM_006724837.1:c.293-176G=	XP_006724900.1:n.293-176G=
XM_006724839.1:c.293-176G=	XP_006724902.1:n.293-176G=
XM_006724841.2:c.-56-176G=	XP_006724904.1:n.-56-176G=
XM_006724842.2:c.-56-176G=	XP_006724905.1:n.-56-176G=
XM_011531189.1:c.293-176G=	XP_011529491.1:n.293-176G=
XM_011531190.1:c.-57+57G=	XP_011529492.1:n.-57+57G=
XM_011531191.1:c.-39+57G=	XP_011529493.1:n.-39+57G=
XM_011531192.1:c.-160+57G=	XP_011529494.1:n.-160+57G=
XR_938511.1:n.596-176G=
XM_006724841.4:c.-56-176G=	XP_006724904.1:n.-56-176G=
XM_006724842.4:c.-56-176G=	XP_006724905.1:n.-56-176G=
XM_011531191.2:c.-39+57G=	XP_011529493.1:n.-39+57G=
XM_017029761.1:c.239-176G=	XP_016885250.1:n.239-176G=
XM_017029762.1:c.293-176G=	XP_016885251.1:n.293-176G=
XM_017029763.1:c.239-176G=	XP_016885252.1:n.239-176G=
XM_017029765.2:c.-56-176G=	XP_016885254.1:n.-56-176G=
XM_024452431.1:c.293-176G=	XP_024308199.1:n.293-176G=
NM_000116.5:c.239-176G= MANE Select	NP_000107.1:n.239-176G=
NM_001303465.2:c.293-176G=	NP_001290394.1:n.293-176G=
NM_181311.4:c.239-176G=	NP_851828.1:n.239-176G=
NM_181312.4:c.239-176G=	NP_851829.1:n.239-176G=
NM_181313.4:c.239-176G=	NP_851830.1:n.239-176G=
NR_024048.3:n.544-176G=