Canonical Allele Identifier: CA401029329

Gene: TSEN54

Linked Data

• dbSNP Id: rs2053431566
• MyVariant Identifiers: chr17:g.73518034C>T (hg19) ; chr17:g.75521953C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521953C>T , CM000679.2:g.75521953C>T	GRCh38
NC_000017.10:g.73518034C>T , CM000679.1:g.73518034C>T	GRCh37
NC_000017.9:g.71029629C>T	NCBI36
NG_013041.1:g.10426C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.872C>T MANE Select	ENSP00000327487.6:p.Ala291Val
ENST00000434205.8:c.569C>T	ENSP00000406559.4:p.Ala190Val
ENST00000545228.3:c.872C>T	ENSP00000438169.3:p.Ala291Val
ENST00000579449.2:n.671C>T
ENST00000580013.6:n.1075C>T
ENST00000679370.1:n.1453C>T
ENST00000679429.1:c.*330C>T	ENSP00000505403.1:n.*330C>T
ENST00000679443.1:n.941C>T
ENST00000679782.1:c.872C>T	ENSP00000505995.1:p.Ala291Val
ENST00000679919.1:n.941C>T
ENST00000679928.1:c.*483C>T	ENSP00000506071.1:n.*483C>T
ENST00000680528.1:n.897C>T
ENST00000680999.1:c.872C>T	ENSP00000504984.1:p.Ala291Val
ENST00000681282.1:c.*118C>T	ENSP00000506339.1:n.*118C>T
ENST00000333213.10:c.872C>T	ENSP00000327487.6:p.Ala291Val
ENST00000578415.1:c.832C>T
ENST00000583173.5:c.459-54C>T	ENSP00000463619.1:n.459-54C>T
NM_207346.2:c.872C>T	NP_997229.2:p.Ala291Val
XM_005257229.2:c.872C>T	XP_005257286.1:p.Ala291Val
XM_006721821.2:c.569C>T	XP_006721884.1:p.Ala190Val
XM_011524616.1:c.872C>T	XP_011522918.1:p.Ala291Val
XM_011524617.1:c.872C>T	XP_011522919.1:p.Ala291Val
XM_011524618.1:c.872C>T	XP_011522920.1:p.Ala291Val
XR_243646.2:n.902C>T
XM_005257229.4:c.872C>T	XP_005257286.1:p.Ala291Val
XR_243646.4:n.908C>T
NM_207346.3:c.872C>T MANE Select	NP_997229.2:p.Ala291Val