Canonical Allele Identifier: CA8764203

Gene: TSEN54

Linked Data

• ClinVar Variation Id: 1653988
• ClinVar RCV Id: RCV002163618
• dbSNP Id: rs767578722
• ExAC: 17:73517535 C / T
• gnomAD v2: 17-73517535-C-T
• gnomAD v4: 17-75521454-C-T
• MyVariant Identifiers: chr17:g.73517535C>T (hg19) ; chr17:g.75521454C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521454C>T , CM000679.2:g.75521454C>T	GRCh38
NC_000017.10:g.73517535C>T , CM000679.1:g.73517535C>T	GRCh37
NC_000017.9:g.71029130C>T	NCBI36
NG_013041.1:g.9927C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.567C>T MANE Select	ENSP00000327487.6:p.Ser189=
ENST00000434205.8:c.264C>T	ENSP00000406559.4:p.Ser88=
ENST00000545228.3:c.567C>T	ENSP00000438169.3:p.Ser189=
ENST00000579449.2:n.366C>T
ENST00000580013.6:n.576C>T
ENST00000583818.2:c.621C>T	ENSP00000461928.2:n.621C>T
ENST00000679370.1:n.954C>T
ENST00000679429.1:c.*25C>T	ENSP00000505403.1:n.*25C>T
ENST00000679443.1:n.442C>T
ENST00000679782.1:c.567C>T	ENSP00000505995.1:p.Ser189=
ENST00000679919.1:n.442C>T
ENST00000679928.1:c.*178C>T	ENSP00000506071.1:n.*178C>T
ENST00000680528.1:n.592C>T
ENST00000680999.1:c.567C>T	ENSP00000504984.1:p.Ser189=
ENST00000681282.1:c.567C>T	ENSP00000506339.1:p.Ser189=
ENST00000333213.10:c.567C>T	ENSP00000327487.6:p.Ser189=
ENST00000578415.1:c.527C>T
ENST00000583173.5:c.402C>T	ENSP00000463619.1:p.Ser134=
ENST00000583818.1:c.516C>T	ENSP00000461928.1:n.516C>T
NM_207346.2:c.567C>T	NP_997229.2:p.Ser189=
XM_005257229.2:c.567C>T	XP_005257286.1:p.Ser189=
XM_006721821.2:c.264C>T	XP_006721884.1:p.Ser88=
XM_011524616.1:c.567C>T	XP_011522918.1:p.Ser189=
XM_011524617.1:c.567C>T	XP_011522919.1:p.Ser189=
XM_011524618.1:c.567C>T	XP_011522920.1:p.Ser189=
XR_243646.2:n.597C>T
XM_005257229.4:c.567C>T	XP_005257286.1:p.Ser189=
XR_243646.4:n.603C>T
NM_207346.3:c.567C>T MANE Select	NP_997229.2:p.Ser189=