Canonical Allele Identifier: CA2275552639

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524473_75524474delinsGA , CM000679.2:g.75524473_75524474delinsGA	GRCh38
NC_000017.10:g.73520554_73520555delinsGA , CM000679.1:g.73520554_73520555delinsGA	GRCh37
NC_000017.9:g.71032149_71032150delinsGA	NCBI36
NG_013041.1:g.12946_12947delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*61_*62delinsGA MANE Select	ENSP00000327487.6:n.*61_*62delinsGA
ENST00000434205.8:c.*61_*62delinsGA	ENSP00000406559.4:n.*61_*62delinsGA
ENST00000545228.3:c.*141_*142delinsGA	ENSP00000438169.3:n.*141_*142delinsGA
ENST00000577197.2:n.840_841delinsGA
ENST00000579449.2:n.2382_2383delinsGA
ENST00000580013.6:n.2786_2787delinsGA
ENST00000679370.1:n.3164_3165delinsGA
ENST00000679429.1:c.*1100_*1101delinsGA	ENSP00000505403.1:n.*1100_*1101delinsGA
ENST00000679443.1:n.1711_1712delinsGA
ENST00000679782.1:c.*341_*342delinsGA	ENSP00000505995.1:n.*341_*342delinsGA
ENST00000679919.1:n.1913_1914delinsGA
ENST00000679928.1:c.*2194_*2195delinsGA	ENSP00000506071.1:n.*2194_*2195delinsGA
ENST00000680999.1:c.*61_*62delinsGA	ENSP00000504984.1:n.*61_*62delinsGA
ENST00000681282.1:c.*1829_*1830delinsGA	ENSP00000506339.1:n.*1829_*1830delinsGA
ENST00000333213.10:c.*61_*62delinsGA	ENSP00000327487.6:n.*61_*62delinsGA
ENST00000545228.2:c.919_920delinsGA
ENST00000577197.1:n.390_391delinsGA
NM_207346.2:c.*61_*62delinsGA	NP_997229.2:n.*61_*62delinsGA
XM_005257229.2:c.*141_*142delinsGA	XP_005257286.1:n.*141_*142delinsGA
XM_006721821.2:c.*141_*142delinsGA	XP_006721884.1:n.*141_*142delinsGA
XM_011524616.1:c.*141_*142delinsGA	XP_011522918.1:n.*141_*142delinsGA
XM_011524618.1:c.*61_*62delinsGA	XP_011522920.1:n.*61_*62delinsGA
XR_243646.2:n.1874_1875delinsGA
XM_005257229.4:c.*141_*142delinsGA	XP_005257286.1:n.*141_*142delinsGA
XR_243646.4:n.1880_1881delinsGA
NM_207346.3:c.*61_*62delinsGA MANE Select	NP_997229.2:n.*61_*62delinsGA