Canonical Allele Identifier: CA2275551384

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522057A= , CM000679.2:g.75522057A=	GRCh38
NC_000017.10:g.73518138A= , CM000679.1:g.73518138A=	GRCh37
NC_000017.9:g.71029733A=	NCBI36
NG_013041.1:g.10530A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.976A= MANE Select	ENSP00000327487.6:p.Asn326=
ENST00000434205.8:c.673A=	ENSP00000406559.4:p.Asn225=
ENST00000545228.3:c.976A=	ENSP00000438169.3:p.Asn326=
ENST00000579449.2:n.775A=
ENST00000580013.6:n.1179A=
ENST00000679370.1:n.1557A=
ENST00000679429.1:c.*434A=	ENSP00000505403.1:n.*434A=
ENST00000679443.1:n.1045A=
ENST00000679782.1:c.976A=	ENSP00000505995.1:p.Asn326=
ENST00000679919.1:n.1045A=
ENST00000679928.1:c.*587A=	ENSP00000506071.1:n.*587A=
ENST00000680528.1:n.1001A=
ENST00000680999.1:c.976A=	ENSP00000504984.1:p.Asn326=
ENST00000681282.1:c.*222A=	ENSP00000506339.1:n.*222A=
ENST00000333213.10:c.976A=	ENSP00000327487.6:p.Asn326=
ENST00000545228.2:c.65A=
ENST00000578415.1:c.936A=
ENST00000583173.5:c.509A=	ENSP00000463619.1:p.Gln170=
NM_207346.2:c.976A=	NP_997229.2:p.Asn326=
XM_005257229.2:c.976A=	XP_005257286.1:p.Asn326=
XM_006721821.2:c.673A=	XP_006721884.1:p.Asn225=
XM_011524616.1:c.976A=	XP_011522918.1:p.Asn326=
XM_011524617.1:c.976A=	XP_011522919.1:p.Asn326=
XM_011524618.1:c.976A=	XP_011522920.1:p.Asn326=
XR_243646.2:n.1006A=
XM_005257229.4:c.976A=	XP_005257286.1:p.Asn326=
XR_243646.4:n.1012A=
NM_207346.3:c.976A= MANE Select	NP_997229.2:p.Asn326=