Canonical Allele Identifier: CA8763969

Gene: TSEN54

Linked Data

• ClinVar Variation Id: 1549790
• ClinVar RCV Id: RCV002189482
• dbSNP Id: rs775687022
• ExAC: 17:73512878 C / T
• gnomAD v2: 17-73512878-C-T
• gnomAD v3: 17-75516797-C-T
• gnomAD v4: 17-75516797-C-T
• MyVariant Identifiers: chr17:g.73512878C>T (hg19) ; chr17:g.75516797C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516797C>T , CM000679.2:g.75516797C>T	GRCh38
NC_000017.10:g.73512878C>T , CM000679.1:g.73512878C>T	GRCh37
NC_000017.9:g.71024473C>T	NCBI36
NG_013041.1:g.5270C>T
NG_033152.1:g.3787G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.108C>T MANE Select	ENSP00000327487.6:p.Arg36=
ENST00000434205.8:c.-82-212C>T	ENSP00000406559.4:n.-82-212C>T
ENST00000545228.3:c.108C>T	ENSP00000438169.3:p.Arg36=
ENST00000579449.2:n.20+181C>T
ENST00000580013.6:n.117C>T
ENST00000583818.2:c.108C>T	ENSP00000461928.2:p.Arg36=
ENST00000679370.1:n.495C>T
ENST00000679429.1:c.108C>T	ENSP00000505403.1:p.Arg36=
ENST00000679782.1:c.108C>T	ENSP00000505995.1:p.Arg36=
ENST00000679928.1:c.108C>T	ENSP00000506071.1:p.Arg36=
ENST00000680528.1:n.133C>T
ENST00000680999.1:c.108C>T	ENSP00000504984.1:p.Arg36=
ENST00000681282.1:c.108C>T	ENSP00000506339.1:p.Arg36=
ENST00000333213.10:c.108C>T	ENSP00000327487.6:p.Arg36=
ENST00000434205.7:c.-82-212C>T	ENSP00000406559.3:n.-82-212C>T
ENST00000580013.5:n.133C>T
ENST00000583173.5:c.56+181C>T	ENSP00000463619.1:n.56+181C>T
ENST00000583454.1:n.143C>T
ENST00000583818.1:c.3C>T	ENSP00000461928.1:p.Arg1=
NM_207346.2:c.108C>T	NP_997229.2:p.Arg36=
XM_005257229.2:c.108C>T	XP_005257286.1:p.Arg36=
XM_006721821.2:c.-196C>T	XP_006721884.1:n.-196C>T
XM_011524616.1:c.108C>T	XP_011522918.1:p.Arg36=
XM_011524617.1:c.108C>T	XP_011522919.1:p.Arg36=
XM_011524618.1:c.108C>T	XP_011522920.1:p.Arg36=
XR_243646.2:n.138C>T
XM_005257229.4:c.108C>T	XP_005257286.1:p.Arg36=
XR_243646.4:n.144C>T
NM_207346.3:c.108C>T MANE Select	NP_997229.2:p.Arg36=