Canonical Allele Identifier: CA2739561955

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524565T>A , CM000679.2:g.75524565T>A	GRCh38
NC_000017.10:g.73520646T>A , CM000679.1:g.73520646T>A	GRCh37
NC_000017.9:g.71032241T>A	NCBI36
NG_013041.1:g.13038T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*153T>A MANE Select	ENSP00000327487.6:n.*153T>A
ENST00000434205.8:c.*153T>A	ENSP00000406559.4:n.*153T>A
ENST00000545228.3:c.*233T>A	ENSP00000438169.3:n.*233T>A
ENST00000577197.2:n.932T>A
ENST00000579449.2:n.2474T>A
ENST00000580013.6:n.2878T>A
ENST00000679370.1:n.3256T>A
ENST00000679429.1:c.*1192T>A	ENSP00000505403.1:n.*1192T>A
ENST00000679443.1:n.1803T>A
ENST00000679782.1:c.*433T>A	ENSP00000505995.1:n.*433T>A
ENST00000679919.1:n.2005T>A
ENST00000679928.1:c.*2286T>A	ENSP00000506071.1:n.*2286T>A
ENST00000680999.1:c.*153T>A	ENSP00000504984.1:n.*153T>A
ENST00000681282.1:c.*1921T>A	ENSP00000506339.1:n.*1921T>A
ENST00000333213.10:c.*153T>A	ENSP00000327487.6:n.*153T>A
ENST00000545228.2:c.1011T>A
ENST00000577197.1:n.482T>A
NM_207346.2:c.*153T>A	NP_997229.2:n.*153T>A
XM_005257229.2:c.*233T>A	XP_005257286.1:n.*233T>A
XM_006721821.2:c.*233T>A	XP_006721884.1:n.*233T>A
XM_011524616.1:c.*233T>A	XP_011522918.1:n.*233T>A
XM_011524618.1:c.*153T>A	XP_011522920.1:n.*153T>A
XR_243646.2:n.1966T>A
XM_005257229.4:c.*233T>A	XP_005257286.1:n.*233T>A
XR_243646.4:n.1972T>A
NM_207346.3:c.*153T>A MANE Select	NP_997229.2:n.*153T>A