Canonical Allele Identifier: CA2275551320

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521953C= , CM000679.2:g.75521953C=	GRCh38
NC_000017.10:g.73518034C= , CM000679.1:g.73518034C=	GRCh37
NC_000017.9:g.71029629C=	NCBI36
NG_013041.1:g.10426C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.872C= MANE Select	ENSP00000327487.6:p.Ala291=
ENST00000434205.8:c.569C=	ENSP00000406559.4:p.Ala190=
ENST00000545228.3:c.872C=	ENSP00000438169.3:p.Ala291=
ENST00000579449.2:n.671C=
ENST00000580013.6:n.1075C=
ENST00000679370.1:n.1453C=
ENST00000679429.1:c.*330C=	ENSP00000505403.1:n.*330C=
ENST00000679443.1:n.941C=
ENST00000679782.1:c.872C=	ENSP00000505995.1:p.Ala291=
ENST00000679919.1:n.941C=
ENST00000679928.1:c.*483C=	ENSP00000506071.1:n.*483C=
ENST00000680528.1:n.897C=
ENST00000680999.1:c.872C=	ENSP00000504984.1:p.Ala291=
ENST00000681282.1:c.*118C=	ENSP00000506339.1:n.*118C=
ENST00000333213.10:c.872C=	ENSP00000327487.6:p.Ala291=
ENST00000578415.1:c.832C=
ENST00000583173.5:c.459-54C=	ENSP00000463619.1:n.459-54C=
NM_207346.2:c.872C=	NP_997229.2:p.Ala291=
XM_005257229.2:c.872C=	XP_005257286.1:p.Ala291=
XM_006721821.2:c.569C=	XP_006721884.1:p.Ala190=
XM_011524616.1:c.872C=	XP_011522918.1:p.Ala291=
XM_011524617.1:c.872C=	XP_011522919.1:p.Ala291=
XM_011524618.1:c.872C=	XP_011522920.1:p.Ala291=
XR_243646.2:n.902C=
XM_005257229.4:c.872C=	XP_005257286.1:p.Ala291=
XR_243646.4:n.908C=
NM_207346.3:c.872C= MANE Select	NP_997229.2:p.Ala291=