Canonical Allele Identifier: CA2275551239

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521816C= , CM000679.2:g.75521816C=	GRCh38
NC_000017.10:g.73517897C= , CM000679.1:g.73517897C=	GRCh37
NC_000017.9:g.71029492C=	NCBI36
NG_013041.1:g.10289C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.735C= MANE Select	ENSP00000327487.6:p.Pro245=
ENST00000434205.8:c.432C=	ENSP00000406559.4:p.Pro144=
ENST00000545228.3:c.735C=	ENSP00000438169.3:p.Pro245=
ENST00000579449.2:n.534C=
ENST00000580013.6:n.938C=
ENST00000583818.2:c.789C=	ENSP00000461928.2:n.789C=
ENST00000679370.1:n.1316C=
ENST00000679429.1:c.*193C=	ENSP00000505403.1:n.*193C=
ENST00000679443.1:n.804C=
ENST00000679782.1:c.735C=	ENSP00000505995.1:p.Pro245=
ENST00000679919.1:n.804C=
ENST00000679928.1:c.*346C=	ENSP00000506071.1:n.*346C=
ENST00000680528.1:n.760C=
ENST00000680999.1:c.735C=	ENSP00000504984.1:p.Pro245=
ENST00000681282.1:c.764C=	ENSP00000506339.1:p.Pro255=
ENST00000333213.10:c.735C=	ENSP00000327487.6:p.Pro245=
ENST00000578415.1:c.695C=
ENST00000583173.5:c.459-191C=	ENSP00000463619.1:n.459-191C=
ENST00000583818.1:c.684C=	ENSP00000461928.1:n.684C=
NM_207346.2:c.735C=	NP_997229.2:p.Pro245=
XM_005257229.2:c.735C=	XP_005257286.1:p.Pro245=
XM_006721821.2:c.432C=	XP_006721884.1:p.Pro144=
XM_011524616.1:c.735C=	XP_011522918.1:p.Pro245=
XM_011524617.1:c.735C=	XP_011522919.1:p.Pro245=
XM_011524618.1:c.735C=	XP_011522920.1:p.Pro245=
XR_243646.2:n.765C=
XM_005257229.4:c.735C=	XP_005257286.1:p.Pro245=
XR_243646.4:n.771C=
NM_207346.3:c.735C= MANE Select	NP_997229.2:p.Pro245=