Canonical Allele Identifier: CA2275552547

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524290A= , CM000679.2:g.75524290A=	GRCh38
NC_000017.10:g.73520371A= , CM000679.1:g.73520371A=	GRCh37
NC_000017.9:g.71031966A=	NCBI36
NG_013041.1:g.12763A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1459A= MANE Select	ENSP00000327487.6:p.Ser487=
ENST00000434205.8:c.1156A=	ENSP00000406559.4:p.Ser386=
ENST00000545228.3:c.1647A=	ENSP00000438169.3:p.Ala549=
ENST00000577197.2:n.657A=
ENST00000579449.2:n.2199A=
ENST00000580013.6:n.2603A=
ENST00000679370.1:n.2981A=
ENST00000679429.1:c.*917A=	ENSP00000505403.1:n.*917A=
ENST00000679443.1:n.1528A=
ENST00000679782.1:c.*158A=	ENSP00000505995.1:n.*158A=
ENST00000679919.1:n.1730A=
ENST00000679928.1:c.*2011A=	ENSP00000506071.1:n.*2011A=
ENST00000680528.1:n.2425A=
ENST00000680999.1:c.1672A=	ENSP00000504984.1:p.Ser558=
ENST00000681282.1:c.*1646A=	ENSP00000506339.1:n.*1646A=
ENST00000333213.10:c.1459A=	ENSP00000327487.6:p.Ser487=
ENST00000545228.2:c.736A=
ENST00000577197.1:n.207A=
ENST00000579449.1:n.656A=
NM_207346.2:c.1459A=	NP_997229.2:p.Ser487=
XM_005257229.2:c.1647A=	XP_005257286.1:p.Ala549=
XM_006721821.2:c.1344A=	XP_006721884.1:p.Ala448=
XM_011524616.1:c.1530A=	XP_011522918.1:p.Ala510=
XM_011524617.1:c.*41A=	XP_011522919.1:n.*41A=
XM_011524618.1:c.1342A=	XP_011522920.1:p.Ser448=
XR_243646.2:n.1691A=
XM_005257229.4:c.1647A=	XP_005257286.1:p.Ala549=
XR_001753015.1:n.87+21T=
XR_001753016.1:n.88+21T=
XR_243646.4:n.1697A=
NM_207346.3:c.1459A= MANE Select	NP_997229.2:p.Ser487=