Canonical Allele Identifier: CA2275552751

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524674_75524676delinsTTA , CM000679.2:g.75524674_75524676delinsTTA	GRCh38
NC_000017.10:g.73520755_73520757delinsTTA , CM000679.1:g.73520755_73520757delinsTTA	GRCh37
NC_000017.9:g.71032350_71032352delinsTTA	NCBI36
NG_013041.1:g.13147_13149delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*262_*264delinsTTA MANE Select	ENSP00000327487.6:n.*262_*264delinsTTA
ENST00000434205.8:c.*262_*264delinsTTA	ENSP00000406559.4:n.*262_*264delinsTTA
ENST00000545228.3:c.*342_*344delinsTTA	ENSP00000438169.3:n.*342_*344delinsTTA
ENST00000577197.2:n.1041_1043delinsTTA
ENST00000579449.2:n.2583_2585delinsTTA
ENST00000580013.6:n.2987_2989delinsTTA
ENST00000679370.1:n.3365_3367delinsTTA
ENST00000679429.1:c.*1301_*1303delinsTTA	ENSP00000505403.1:n.*1301_*1303delinsTTA
ENST00000679443.1:n.1912_1914delinsTTA
ENST00000679782.1:c.*542_*544delinsTTA	ENSP00000505995.1:n.*542_*544delinsTTA
ENST00000679919.1:n.2114_2116delinsTTA
ENST00000679928.1:c.*2395_*2397delinsTTA	ENSP00000506071.1:n.*2395_*2397delinsTTA
ENST00000680999.1:c.*262_*264delinsTTA	ENSP00000504984.1:n.*262_*264delinsTTA
ENST00000681282.1:c.*2030_*2032delinsTTA	ENSP00000506339.1:n.*2030_*2032delinsTTA
ENST00000333213.10:c.*262_*264delinsTTA	ENSP00000327487.6:n.*262_*264delinsTTA
ENST00000545228.2:c.1120_1122delinsTTA
ENST00000577197.1:n.591_593delinsTTA
NM_207346.2:c.*262_*264delinsTTA	NP_997229.2:n.*262_*264delinsTTA
XM_005257229.2:c.*342_*344delinsTTA	XP_005257286.1:n.*342_*344delinsTTA
XM_006721821.2:c.*342_*344delinsTTA	XP_006721884.1:n.*342_*344delinsTTA
XM_011524616.1:c.*342_*344delinsTTA	XP_011522918.1:n.*342_*344delinsTTA
XM_011524618.1:c.*262_*264delinsTTA	XP_011522920.1:n.*262_*264delinsTTA
XR_243646.2:n.2075_2077delinsTTA
XM_005257229.4:c.*342_*344delinsTTA	XP_005257286.1:n.*342_*344delinsTTA
XR_243646.4:n.2081_2083delinsTTA
NM_207346.3:c.*262_*264delinsTTA MANE Select	NP_997229.2:n.*262_*264delinsTTA