Canonical Allele Identifier: CA2275551192

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521735C= , CM000679.2:g.75521735C=	GRCh38
NC_000017.10:g.73517816C= , CM000679.1:g.73517816C=	GRCh37
NC_000017.9:g.71029411C=	NCBI36
NG_013041.1:g.10208C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.654C= MANE Select	ENSP00000327487.6:p.Asp218=
ENST00000434205.8:c.351C=	ENSP00000406559.4:p.Asp117=
ENST00000545228.3:c.654C=	ENSP00000438169.3:p.Asp218=
ENST00000579449.2:n.453C=
ENST00000580013.6:n.857C=
ENST00000583818.2:c.708C=	ENSP00000461928.2:n.708C=
ENST00000679370.1:n.1235C=
ENST00000679429.1:c.*112C=	ENSP00000505403.1:n.*112C=
ENST00000679443.1:n.723C=
ENST00000679782.1:c.654C=	ENSP00000505995.1:p.Asp218=
ENST00000679919.1:n.723C=
ENST00000679928.1:c.*265C=	ENSP00000506071.1:n.*265C=
ENST00000680528.1:n.679C=
ENST00000680999.1:c.654C=	ENSP00000504984.1:p.Asp218=
ENST00000681282.1:c.683C=	ENSP00000506339.1:p.Thr228=
ENST00000333213.10:c.654C=	ENSP00000327487.6:p.Asp218=
ENST00000578415.1:c.614C=
ENST00000583173.5:c.458+225C=	ENSP00000463619.1:n.458+225C=
ENST00000583818.1:c.603C=	ENSP00000461928.1:n.603C=
NM_207346.2:c.654C=	NP_997229.2:p.Asp218=
XM_005257229.2:c.654C=	XP_005257286.1:p.Asp218=
XM_006721821.2:c.351C=	XP_006721884.1:p.Asp117=
XM_011524616.1:c.654C=	XP_011522918.1:p.Asp218=
XM_011524617.1:c.654C=	XP_011522919.1:p.Asp218=
XM_011524618.1:c.654C=	XP_011522920.1:p.Asp218=
XR_243646.2:n.684C=
XM_005257229.4:c.654C=	XP_005257286.1:p.Asp218=
XR_243646.4:n.690C=
NM_207346.3:c.654C= MANE Select	NP_997229.2:p.Asp218=