Canonical Allele Identifier: CA502046291

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73518146T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522065T>G , CM000679.2:g.75522065T>G	GRCh38
NC_000017.10:g.73518146T>G , CM000679.1:g.73518146T>G	GRCh37
NC_000017.9:g.71029741T>G	NCBI36
NG_013041.1:g.10538T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.984T>G MANE Select	ENSP00000327487.6:p.Ala328=
ENST00000434205.8:c.681T>G	ENSP00000406559.4:p.Ala227=
ENST00000545228.3:c.984T>G	ENSP00000438169.3:p.Ala328=
ENST00000579449.2:n.783T>G
ENST00000580013.6:n.1187T>G
ENST00000679370.1:n.1565T>G
ENST00000679429.1:c.*442T>G	ENSP00000505403.1:n.*442T>G
ENST00000679443.1:n.1053T>G
ENST00000679782.1:c.984T>G	ENSP00000505995.1:p.Ala328=
ENST00000679919.1:n.1053T>G
ENST00000679928.1:c.*595T>G	ENSP00000506071.1:n.*595T>G
ENST00000680528.1:n.1009T>G
ENST00000680999.1:c.984T>G	ENSP00000504984.1:p.Ala328=
ENST00000681282.1:c.*230T>G	ENSP00000506339.1:n.*230T>G
ENST00000333213.10:c.984T>G	ENSP00000327487.6:p.Ala328=
ENST00000545228.2:c.73T>G
ENST00000578415.1:c.944T>G
ENST00000583173.5:c.517T>G	ENSP00000463619.1:p.Trp173Gly
NM_207346.2:c.984T>G	NP_997229.2:p.Ala328=
XM_005257229.2:c.984T>G	XP_005257286.1:p.Ala328=
XM_006721821.2:c.681T>G	XP_006721884.1:p.Ala227=
XM_011524616.1:c.984T>G	XP_011522918.1:p.Ala328=
XM_011524617.1:c.984T>G	XP_011522919.1:p.Ala328=
XM_011524618.1:c.984T>G	XP_011522920.1:p.Ala328=
XR_243646.2:n.1014T>G
XM_005257229.4:c.984T>G	XP_005257286.1:p.Ala328=
XR_243646.4:n.1020T>G
NM_207346.3:c.984T>G MANE Select	NP_997229.2:p.Ala328=