Canonical Allele Identifier: CA2275552695

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524579T= , CM000679.2:g.75524579T=	GRCh38
NC_000017.10:g.73520660T= , CM000679.1:g.73520660T=	GRCh37
NC_000017.9:g.71032255T=	NCBI36
NG_013041.1:g.13052T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*167T= MANE Select	ENSP00000327487.6:n.*167T=
ENST00000434205.8:c.*167T=	ENSP00000406559.4:n.*167T=
ENST00000545228.3:c.*247T=	ENSP00000438169.3:n.*247T=
ENST00000577197.2:n.946T=
ENST00000579449.2:n.2488T=
ENST00000580013.6:n.2892T=
ENST00000679370.1:n.3270T=
ENST00000679429.1:c.*1206T=	ENSP00000505403.1:n.*1206T=
ENST00000679443.1:n.1817T=
ENST00000679782.1:c.*447T=	ENSP00000505995.1:n.*447T=
ENST00000679919.1:n.2019T=
ENST00000679928.1:c.*2300T=	ENSP00000506071.1:n.*2300T=
ENST00000680999.1:c.*167T=	ENSP00000504984.1:n.*167T=
ENST00000681282.1:c.*1935T=	ENSP00000506339.1:n.*1935T=
ENST00000333213.10:c.*167T=	ENSP00000327487.6:n.*167T=
ENST00000545228.2:c.1025T=
ENST00000577197.1:n.496T=
NM_207346.2:c.*167T=	NP_997229.2:n.*167T=
XM_005257229.2:c.*247T=	XP_005257286.1:n.*247T=
XM_006721821.2:c.*247T=	XP_006721884.1:n.*247T=
XM_011524616.1:c.*247T=	XP_011522918.1:n.*247T=
XM_011524618.1:c.*167T=	XP_011522920.1:n.*167T=
XR_243646.2:n.1980T=
XM_005257229.4:c.*247T=	XP_005257286.1:n.*247T=
XR_243646.4:n.1986T=
NM_207346.3:c.*167T= MANE Select	NP_997229.2:n.*167T=