Canonical Allele Identifier: CA401029243

Gene: TSEN54

Linked Data

• dbSNP Id: rs1439782684
• gnomAD v2: 17-73518012-G-A
• gnomAD v4: 17-75521931-G-A
• MyVariant Identifiers: chr17:g.73518012G>A (hg19) ; chr17:g.75521931G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521931G>A , CM000679.2:g.75521931G>A	GRCh38
NC_000017.10:g.73518012G>A , CM000679.1:g.73518012G>A	GRCh37
NC_000017.9:g.71029607G>A	NCBI36
NG_013041.1:g.10404G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.850G>A MANE Select	ENSP00000327487.6:p.Ala284Thr
ENST00000434205.8:c.547G>A	ENSP00000406559.4:p.Ala183Thr
ENST00000545228.3:c.850G>A	ENSP00000438169.3:p.Ala284Thr
ENST00000579449.2:n.649G>A
ENST00000580013.6:n.1053G>A
ENST00000679370.1:n.1431G>A
ENST00000679429.1:c.*308G>A	ENSP00000505403.1:n.*308G>A
ENST00000679443.1:n.919G>A
ENST00000679782.1:c.850G>A	ENSP00000505995.1:p.Ala284Thr
ENST00000679919.1:n.919G>A
ENST00000679928.1:c.*461G>A	ENSP00000506071.1:n.*461G>A
ENST00000680528.1:n.875G>A
ENST00000680999.1:c.850G>A	ENSP00000504984.1:p.Ala284Thr
ENST00000681282.1:c.*96G>A	ENSP00000506339.1:n.*96G>A
ENST00000333213.10:c.850G>A	ENSP00000327487.6:p.Ala284Thr
ENST00000578415.1:c.810G>A
ENST00000583173.5:c.459-76G>A	ENSP00000463619.1:n.459-76G>A
NM_207346.2:c.850G>A	NP_997229.2:p.Ala284Thr
XM_005257229.2:c.850G>A	XP_005257286.1:p.Ala284Thr
XM_006721821.2:c.547G>A	XP_006721884.1:p.Ala183Thr
XM_011524616.1:c.850G>A	XP_011522918.1:p.Ala284Thr
XM_011524617.1:c.850G>A	XP_011522919.1:p.Ala284Thr
XM_011524618.1:c.850G>A	XP_011522920.1:p.Ala284Thr
XR_243646.2:n.880G>A
XM_005257229.4:c.850G>A	XP_005257286.1:p.Ala284Thr
XR_243646.4:n.886G>A
NM_207346.3:c.850G>A MANE Select	NP_997229.2:p.Ala284Thr