Canonical Allele Identifier: CA2275551230

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521803C= , CM000679.2:g.75521803C=	GRCh38
NC_000017.10:g.73517884C= , CM000679.1:g.73517884C=	GRCh37
NC_000017.9:g.71029479C=	NCBI36
NG_013041.1:g.10276C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.722C= MANE Select	ENSP00000327487.6:p.Pro241=
ENST00000434205.8:c.419C=	ENSP00000406559.4:p.Pro140=
ENST00000545228.3:c.722C=	ENSP00000438169.3:p.Pro241=
ENST00000579449.2:n.521C=
ENST00000580013.6:n.925C=
ENST00000583818.2:c.776C=	ENSP00000461928.2:n.776C=
ENST00000679370.1:n.1303C=
ENST00000679429.1:c.*180C=	ENSP00000505403.1:n.*180C=
ENST00000679443.1:n.791C=
ENST00000679782.1:c.722C=	ENSP00000505995.1:p.Pro241=
ENST00000679919.1:n.791C=
ENST00000679928.1:c.*333C=	ENSP00000506071.1:n.*333C=
ENST00000680528.1:n.747C=
ENST00000680999.1:c.722C=	ENSP00000504984.1:p.Pro241=
ENST00000681282.1:c.751C=	ENSP00000506339.1:p.Gln251=
ENST00000333213.10:c.722C=	ENSP00000327487.6:p.Pro241=
ENST00000578415.1:c.682C=
ENST00000583173.5:c.459-204C=	ENSP00000463619.1:n.459-204C=
ENST00000583818.1:c.671C=	ENSP00000461928.1:n.671C=
NM_207346.2:c.722C=	NP_997229.2:p.Pro241=
XM_005257229.2:c.722C=	XP_005257286.1:p.Pro241=
XM_006721821.2:c.419C=	XP_006721884.1:p.Pro140=
XM_011524616.1:c.722C=	XP_011522918.1:p.Pro241=
XM_011524617.1:c.722C=	XP_011522919.1:p.Pro241=
XM_011524618.1:c.722C=	XP_011522920.1:p.Pro241=
XR_243646.2:n.752C=
XM_005257229.4:c.722C=	XP_005257286.1:p.Pro241=
XR_243646.4:n.758C=
NM_207346.3:c.722C= MANE Select	NP_997229.2:p.Pro241=