Canonical Allele Identifier: CA2275548470

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516803T= , CM000679.2:g.75516803T=	GRCh38
NC_000017.10:g.73512884T= , CM000679.1:g.73512884T=	GRCh37
NC_000017.9:g.71024479T=	NCBI36
NG_013041.1:g.5276T=
NG_033152.1:g.3781A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.114T= MANE Select	ENSP00000327487.6:p.His38=
ENST00000434205.8:c.-82-206T=	ENSP00000406559.4:n.-82-206T=
ENST00000545228.3:c.114T=	ENSP00000438169.3:p.His38=
ENST00000579449.2:n.20+187T=
ENST00000580013.6:n.123T=
ENST00000583818.2:c.114T=	ENSP00000461928.2:p.His38=
ENST00000679370.1:n.501T=
ENST00000679429.1:c.114T=	ENSP00000505403.1:p.His38=
ENST00000679782.1:c.114T=	ENSP00000505995.1:p.His38=
ENST00000679928.1:c.114T=	ENSP00000506071.1:p.His38=
ENST00000680528.1:n.139T=
ENST00000680999.1:c.114T=	ENSP00000504984.1:p.His38=
ENST00000681282.1:c.114T=	ENSP00000506339.1:p.His38=
ENST00000333213.10:c.114T=	ENSP00000327487.6:p.His38=
ENST00000434205.7:c.-82-206T=	ENSP00000406559.3:n.-82-206T=
ENST00000580013.5:n.139T=
ENST00000583173.5:c.56+187T=	ENSP00000463619.1:n.56+187T=
ENST00000583454.1:n.149T=
ENST00000583818.1:c.9T=	ENSP00000461928.1:p.His3=
NM_207346.2:c.114T=	NP_997229.2:p.His38=
XM_005257229.2:c.114T=	XP_005257286.1:p.His38=
XM_006721821.2:c.-190T=	XP_006721884.1:n.-190T=
XM_011524616.1:c.114T=	XP_011522918.1:p.His38=
XM_011524617.1:c.114T=	XP_011522919.1:p.His38=
XM_011524618.1:c.114T=	XP_011522920.1:p.His38=
XR_243646.2:n.144T=
XM_005257229.4:c.114T=	XP_005257286.1:p.His38=
XR_243646.4:n.150T=
NM_207346.3:c.114T= MANE Select	NP_997229.2:p.His38=