Canonical Allele Identifier: CA2160598115

Gene: TDRD9

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.104042739C= , CM000676.2:g.104042739C=	GRCh38
NC_000014.8:g.104509076C= , CM000676.1:g.104509076C=	GRCh37
NC_000014.7:g.103578829C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_153046.3:c.3974+552C= MANE Select	NP_694591.2:n.3974+552C=
ENST00000409874.9:c.3974+552C= MANE Select	ENSP00000387303.4:n.3974+552C=
NM_153046.2:c.3974+552C=	NP_694591.2:n.3974+552C=
ENST00000339063.6:c.*484+552C=	ENSP00000343545.6:n.*484+552C=
ENST00000409874.8:c.3974+552C=	ENSP00000387303.4:n.3974+552C=
ENST00000557332.5:c.2580+552C=
XM_005267309.2:c.3818+552C=	XP_005267366.1:n.3818+552C=
XM_005267309.4:c.3818+552C=	XP_005267366.1:n.3818+552C=
XM_006720019.2:c.3974+552C=	XP_006720082.1:n.3974+552C=
XM_006720019.3:c.3974+552C=	XP_006720082.1:n.3974+552C=
XM_006720020.2:c.3893+552C=	XP_006720083.1:n.3893+552C=
XM_006720020.3:c.3893+552C=	XP_006720083.1:n.3893+552C=
XM_011536396.1:c.3974+552C=	XP_011534698.1:n.3974+552C=
XM_011536397.1:c.3869+552C=	XP_011534699.1:n.3869+552C=
XM_011536397.2:c.3869+552C=	XP_011534699.1:n.3869+552C=
XM_011536398.1:c.3860+552C=	XP_011534700.1:n.3860+552C=
XM_011536398.3:c.3860+552C=	XP_011534700.1:n.3860+552C=
XM_011536399.1:c.3776+552C=	XP_011534701.1:n.3776+552C=
XM_011536400.1:c.3713+552C=	XP_011534702.1:n.3713+552C=
XM_011536400.2:c.3713+552C=	XP_011534702.1:n.3713+552C=
XM_011536401.1:c.3287+552C=	XP_011534703.1:n.3287+552C=
XM_011536401.3:c.3287+552C=	XP_011534703.1:n.3287+552C=
XM_011536402.1:c.2888+552C=	XP_011534704.1:n.2888+552C=
XM_011536402.2:c.2888+552C=	XP_011534704.1:n.2888+552C=
XM_017020955.2:c.2732+552C=	XP_016876444.1:n.2732+552C=