Canonical Allele Identifier: CA2576389066

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524439T>A , CM000679.2:g.75524439T>A	GRCh38
NC_000017.10:g.73520520T>A , CM000679.1:g.73520520T>A	GRCh37
NC_000017.9:g.71032115T>A	NCBI36
NG_013041.1:g.12912T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*27T>A MANE Select	ENSP00000327487.6:n.*27T>A
ENST00000434205.8:c.*27T>A	ENSP00000406559.4:n.*27T>A
ENST00000545228.3:c.*107T>A	ENSP00000438169.3:n.*107T>A
ENST00000577197.2:n.806T>A
ENST00000579449.2:n.2348T>A
ENST00000580013.6:n.2752T>A
ENST00000679370.1:n.3130T>A
ENST00000679429.1:c.*1066T>A	ENSP00000505403.1:n.*1066T>A
ENST00000679443.1:n.1677T>A
ENST00000679782.1:c.*307T>A	ENSP00000505995.1:n.*307T>A
ENST00000679919.1:n.1879T>A
ENST00000679928.1:c.*2160T>A	ENSP00000506071.1:n.*2160T>A
ENST00000680999.1:c.*27T>A	ENSP00000504984.1:n.*27T>A
ENST00000681282.1:c.*1795T>A	ENSP00000506339.1:n.*1795T>A
ENST00000333213.10:c.*27T>A	ENSP00000327487.6:n.*27T>A
ENST00000545228.2:c.885T>A
ENST00000577197.1:n.356T>A
NM_207346.2:c.*27T>A	NP_997229.2:n.*27T>A
XM_005257229.2:c.*107T>A	XP_005257286.1:n.*107T>A
XM_006721821.2:c.*107T>A	XP_006721884.1:n.*107T>A
XM_011524616.1:c.*107T>A	XP_011522918.1:n.*107T>A
XM_011524618.1:c.*27T>A	XP_011522920.1:n.*27T>A
XR_243646.2:n.1840T>A
XM_005257229.4:c.*107T>A	XP_005257286.1:n.*107T>A
XR_243646.4:n.1846T>A
NM_207346.3:c.*27T>A MANE Select	NP_997229.2:n.*27T>A