Canonical Allele Identifier: CA2275548445

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516746C= , CM000679.2:g.75516746C=	GRCh38
NC_000017.10:g.73512827C= , CM000679.1:g.73512827C=	GRCh37
NC_000017.9:g.71024422C=	NCBI36
NG_013041.1:g.5219C=
NG_033152.1:g.3838G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.57C= MANE Select	ENSP00000327487.6:p.Ser19=
ENST00000434205.8:c.-82-263C=	ENSP00000406559.4:n.-82-263C=
ENST00000545228.3:c.57C=	ENSP00000438169.3:p.Ser19=
ENST00000579449.2:n.20+130C=
ENST00000580013.6:n.66C=
ENST00000583818.2:c.57C=	ENSP00000461928.2:p.Ser19=
ENST00000679370.1:n.444C=
ENST00000679429.1:c.57C=	ENSP00000505403.1:p.Ser19=
ENST00000679782.1:c.57C=	ENSP00000505995.1:p.Ser19=
ENST00000679928.1:c.57C=	ENSP00000506071.1:p.Ser19=
ENST00000680528.1:n.82C=
ENST00000680999.1:c.57C=	ENSP00000504984.1:p.Ser19=
ENST00000681282.1:c.57C=	ENSP00000506339.1:p.Ser19=
ENST00000333213.10:c.57C=	ENSP00000327487.6:p.Ser19=
ENST00000434205.7:c.-82-263C=	ENSP00000406559.3:n.-82-263C=
ENST00000580013.5:n.82C=
ENST00000583173.5:c.56+130C=	ENSP00000463619.1:n.56+130C=
ENST00000583454.1:n.92C=
NM_207346.2:c.57C=	NP_997229.2:p.Ser19=
XM_005257229.2:c.57C=	XP_005257286.1:p.Ser19=
XM_006721821.2:c.-247C=	XP_006721884.1:n.-247C=
XM_011524616.1:c.57C=	XP_011522918.1:p.Ser19=
XM_011524617.1:c.57C=	XP_011522919.1:p.Ser19=
XM_011524618.1:c.57C=	XP_011522920.1:p.Ser19=
XR_243646.2:n.87C=
XM_005257229.4:c.57C=	XP_005257286.1:p.Ser19=
XR_243646.4:n.93C=
NM_207346.3:c.57C= MANE Select	NP_997229.2:p.Ser19=