Canonical Allele Identifier: CA401029452

Gene: TSEN54

Linked Data

• dbSNP Id: rs1350195436
• gnomAD v2: 17-73518082-C-T
• gnomAD v3: 17-75522001-C-T
• gnomAD v4: 17-75522001-C-T
• MyVariant Identifiers: chr17:g.73518082C>T (hg19) ; chr17:g.75522001C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522001C>T , CM000679.2:g.75522001C>T	GRCh38
NC_000017.10:g.73518082C>T , CM000679.1:g.73518082C>T	GRCh37
NC_000017.9:g.71029677C>T	NCBI36
NG_013041.1:g.10474C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.920C>T MANE Select	ENSP00000327487.6:p.Ala307Val
ENST00000434205.8:c.617C>T	ENSP00000406559.4:p.Ala206Val
ENST00000545228.3:c.920C>T	ENSP00000438169.3:p.Ala307Val
ENST00000579449.2:n.719C>T
ENST00000580013.6:n.1123C>T
ENST00000679370.1:n.1501C>T
ENST00000679429.1:c.*378C>T	ENSP00000505403.1:n.*378C>T
ENST00000679443.1:n.989C>T
ENST00000679782.1:c.920C>T	ENSP00000505995.1:p.Ala307Val
ENST00000679919.1:n.989C>T
ENST00000679928.1:c.*531C>T	ENSP00000506071.1:n.*531C>T
ENST00000680528.1:n.945C>T
ENST00000680999.1:c.920C>T	ENSP00000504984.1:p.Ala307Val
ENST00000681282.1:c.*166C>T	ENSP00000506339.1:n.*166C>T
ENST00000333213.10:c.920C>T	ENSP00000327487.6:p.Ala307Val
ENST00000545228.2:c.9C>T
ENST00000578415.1:c.880C>T
ENST00000583173.5:c.459-6C>T	ENSP00000463619.1:n.459-6C>T
NM_207346.2:c.920C>T	NP_997229.2:p.Ala307Val
XM_005257229.2:c.920C>T	XP_005257286.1:p.Ala307Val
XM_006721821.2:c.617C>T	XP_006721884.1:p.Ala206Val
XM_011524616.1:c.920C>T	XP_011522918.1:p.Ala307Val
XM_011524617.1:c.920C>T	XP_011522919.1:p.Ala307Val
XM_011524618.1:c.920C>T	XP_011522920.1:p.Ala307Val
XR_243646.2:n.950C>T
XM_005257229.4:c.920C>T	XP_005257286.1:p.Ala307Val
XR_243646.4:n.956C>T
NM_207346.3:c.920C>T MANE Select	NP_997229.2:p.Ala307Val