Canonical Allele Identifier: CA401029395

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75521976-G-T
• MyVariant Identifiers: chr17:g.73518057G>T (hg19) ; chr17:g.75521976G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521976G>T , CM000679.2:g.75521976G>T	GRCh38
NC_000017.10:g.73518057G>T , CM000679.1:g.73518057G>T	GRCh37
NC_000017.9:g.71029652G>T	NCBI36
NG_013041.1:g.10449G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.895G>T MANE Select	ENSP00000327487.6:p.Glu299Ter
ENST00000434205.8:c.592G>T	ENSP00000406559.4:p.Glu198Ter
ENST00000545228.3:c.895G>T	ENSP00000438169.3:p.Glu299Ter
ENST00000579449.2:n.694G>T
ENST00000580013.6:n.1098G>T
ENST00000679370.1:n.1476G>T
ENST00000679429.1:c.*353G>T	ENSP00000505403.1:n.*353G>T
ENST00000679443.1:n.964G>T
ENST00000679782.1:c.895G>T	ENSP00000505995.1:p.Glu299Ter
ENST00000679919.1:n.964G>T
ENST00000679928.1:c.*506G>T	ENSP00000506071.1:n.*506G>T
ENST00000680528.1:n.920G>T
ENST00000680999.1:c.895G>T	ENSP00000504984.1:p.Glu299Ter
ENST00000681282.1:c.*141G>T	ENSP00000506339.1:n.*141G>T
ENST00000333213.10:c.895G>T	ENSP00000327487.6:p.Glu299Ter
ENST00000578415.1:c.855G>T
ENST00000583173.5:c.459-31G>T	ENSP00000463619.1:n.459-31G>T
NM_207346.2:c.895G>T	NP_997229.2:p.Glu299Ter
XM_005257229.2:c.895G>T	XP_005257286.1:p.Glu299Ter
XM_006721821.2:c.592G>T	XP_006721884.1:p.Glu198Ter
XM_011524616.1:c.895G>T	XP_011522918.1:p.Glu299Ter
XM_011524617.1:c.895G>T	XP_011522919.1:p.Glu299Ter
XM_011524618.1:c.895G>T	XP_011522920.1:p.Glu299Ter
XR_243646.2:n.925G>T
XM_005257229.4:c.895G>T	XP_005257286.1:p.Glu299Ter
XR_243646.4:n.931G>T
NM_207346.3:c.895G>T MANE Select	NP_997229.2:p.Glu299Ter