Canonical Allele Identifier: CA401029017

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517950C>A (hg19) ; chr17:g.75521869C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521869C>A , CM000679.2:g.75521869C>A	GRCh38
NC_000017.10:g.73517950C>A , CM000679.1:g.73517950C>A	GRCh37
NC_000017.9:g.71029545C>A	NCBI36
NG_013041.1:g.10342C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.788C>A MANE Select	ENSP00000327487.6:p.Ser263Tyr
ENST00000434205.8:c.485C>A	ENSP00000406559.4:p.Ser162Tyr
ENST00000545228.3:c.788C>A	ENSP00000438169.3:p.Ser263Tyr
ENST00000579449.2:n.587C>A
ENST00000580013.6:n.991C>A
ENST00000583818.2:c.842C>A	ENSP00000461928.2:n.842C>A
ENST00000679370.1:n.1369C>A
ENST00000679429.1:c.*246C>A	ENSP00000505403.1:n.*246C>A
ENST00000679443.1:n.857C>A
ENST00000679782.1:c.788C>A	ENSP00000505995.1:p.Ser263Tyr
ENST00000679919.1:n.857C>A
ENST00000679928.1:c.*399C>A	ENSP00000506071.1:n.*399C>A
ENST00000680528.1:n.813C>A
ENST00000680999.1:c.788C>A	ENSP00000504984.1:p.Ser263Tyr
ENST00000681282.1:c.*34C>A	ENSP00000506339.1:n.*34C>A
ENST00000333213.10:c.788C>A	ENSP00000327487.6:p.Ser263Tyr
ENST00000578415.1:c.748C>A
ENST00000583173.5:c.459-138C>A	ENSP00000463619.1:n.459-138C>A
ENST00000583818.1:c.737C>A	ENSP00000461928.1:n.737C>A
NM_207346.2:c.788C>A	NP_997229.2:p.Ser263Tyr
XM_005257229.2:c.788C>A	XP_005257286.1:p.Ser263Tyr
XM_006721821.2:c.485C>A	XP_006721884.1:p.Ser162Tyr
XM_011524616.1:c.788C>A	XP_011522918.1:p.Ser263Tyr
XM_011524617.1:c.788C>A	XP_011522919.1:p.Ser263Tyr
XM_011524618.1:c.788C>A	XP_011522920.1:p.Ser263Tyr
XR_243646.2:n.818C>A
XM_005257229.4:c.788C>A	XP_005257286.1:p.Ser263Tyr
XR_243646.4:n.824C>A
NM_207346.3:c.788C>A MANE Select	NP_997229.2:p.Ser263Tyr