Canonical Allele Identifier: CA294078535

Gene: TSEN54

Linked Data

• dbSNP Id: rs138028816
• gnomAD v3: 17-75521459-A-T
• gnomAD v4: 17-75521459-A-T
• MyVariant Identifiers: chr17:g.73517540A>T (hg19) ; chr17:g.75521459A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521459A>T , CM000679.2:g.75521459A>T	GRCh38
NC_000017.10:g.73517540A>T , CM000679.1:g.73517540A>T	GRCh37
NC_000017.9:g.71029135A>T	NCBI36
NG_013041.1:g.9932A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.572A>T MANE Select	ENSP00000327487.6:p.Gln191Leu
ENST00000434205.8:c.269A>T	ENSP00000406559.4:p.Gln90Leu
ENST00000545228.3:c.572A>T	ENSP00000438169.3:p.Gln191Leu
ENST00000579449.2:n.371A>T
ENST00000580013.6:n.581A>T
ENST00000583818.2:c.626A>T	ENSP00000461928.2:n.626A>T
ENST00000679370.1:n.959A>T
ENST00000679429.1:c.*30A>T	ENSP00000505403.1:n.*30A>T
ENST00000679443.1:n.447A>T
ENST00000679782.1:c.572A>T	ENSP00000505995.1:p.Gln191Leu
ENST00000679919.1:n.447A>T
ENST00000679928.1:c.*183A>T	ENSP00000506071.1:n.*183A>T
ENST00000680528.1:n.597A>T
ENST00000680999.1:c.572A>T	ENSP00000504984.1:p.Gln191Leu
ENST00000681282.1:c.572A>T	ENSP00000506339.1:p.Gln191Leu
ENST00000333213.10:c.572A>T	ENSP00000327487.6:p.Gln191Leu
ENST00000578415.1:c.532A>T
ENST00000583173.5:c.407A>T	ENSP00000463619.1:p.Gln136Leu
ENST00000583818.1:c.521A>T	ENSP00000461928.1:n.521A>T
NM_207346.2:c.572A>T	NP_997229.2:p.Gln191Leu
XM_005257229.2:c.572A>T	XP_005257286.1:p.Gln191Leu
XM_006721821.2:c.269A>T	XP_006721884.1:p.Gln90Leu
XM_011524616.1:c.572A>T	XP_011522918.1:p.Gln191Leu
XM_011524617.1:c.572A>T	XP_011522919.1:p.Gln191Leu
XM_011524618.1:c.572A>T	XP_011522920.1:p.Gln191Leu
XR_243646.2:n.602A>T
XM_005257229.4:c.572A>T	XP_005257286.1:p.Gln191Leu
XR_243646.4:n.608A>T
NM_207346.3:c.572A>T MANE Select	NP_997229.2:p.Gln191Leu