Canonical Allele Identifier: CA2275552708

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524601A= , CM000679.2:g.75524601A=	GRCh38
NC_000017.10:g.73520682A= , CM000679.1:g.73520682A=	GRCh37
NC_000017.9:g.71032277A=	NCBI36
NG_013041.1:g.13074A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*189A= MANE Select	ENSP00000327487.6:n.*189A=
ENST00000434205.8:c.*189A=	ENSP00000406559.4:n.*189A=
ENST00000545228.3:c.*269A=	ENSP00000438169.3:n.*269A=
ENST00000577197.2:n.968A=
ENST00000579449.2:n.2510A=
ENST00000580013.6:n.2914A=
ENST00000679370.1:n.3292A=
ENST00000679429.1:c.*1228A=	ENSP00000505403.1:n.*1228A=
ENST00000679443.1:n.1839A=
ENST00000679782.1:c.*469A=	ENSP00000505995.1:n.*469A=
ENST00000679919.1:n.2041A=
ENST00000679928.1:c.*2322A=	ENSP00000506071.1:n.*2322A=
ENST00000680999.1:c.*189A=	ENSP00000504984.1:n.*189A=
ENST00000681282.1:c.*1957A=	ENSP00000506339.1:n.*1957A=
ENST00000333213.10:c.*189A=	ENSP00000327487.6:n.*189A=
ENST00000545228.2:c.1047A=
ENST00000577197.1:n.518A=
NM_207346.2:c.*189A=	NP_997229.2:n.*189A=
XM_005257229.2:c.*269A=	XP_005257286.1:n.*269A=
XM_006721821.2:c.*269A=	XP_006721884.1:n.*269A=
XM_011524616.1:c.*269A=	XP_011522918.1:n.*269A=
XM_011524618.1:c.*189A=	XP_011522920.1:n.*189A=
XR_243646.2:n.2002A=
XM_005257229.4:c.*269A=	XP_005257286.1:n.*269A=
XR_243646.4:n.2008A=
NM_207346.3:c.*189A= MANE Select	NP_997229.2:n.*189A=