Canonical Allele Identifier: CA401027876

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73515101G>T (hg19) ; chr17:g.75519020G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75519020G>T , CM000679.2:g.75519020G>T	GRCh38
NC_000017.10:g.73515101G>T , CM000679.1:g.73515101G>T	GRCh37
NC_000017.9:g.71026696G>T	NCBI36
NG_013041.1:g.7493G>T
NG_033152.1:g.1564C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.494G>T MANE Select	ENSP00000327487.6:p.Gly165Val
ENST00000434205.8:c.191G>T	ENSP00000406559.4:p.Gly64Val
ENST00000545228.3:c.494G>T	ENSP00000438169.3:p.Gly165Val
ENST00000579449.2:n.293G>T
ENST00000580013.6:n.503G>T
ENST00000583818.2:c.494G>T	ENSP00000461928.2:p.Gly165Val
ENST00000679370.1:n.881G>T
ENST00000679429.1:c.486G>T	ENSP00000505403.1:p.Gly162=
ENST00000679443.1:n.369G>T
ENST00000679782.1:c.494G>T	ENSP00000505995.1:p.Gly165Val
ENST00000679919.1:n.369G>T
ENST00000679928.1:c.494G>T	ENSP00000506071.1:p.Gly165Val
ENST00000680528.1:n.519G>T
ENST00000680999.1:c.494G>T	ENSP00000504984.1:p.Gly165Val
ENST00000681282.1:c.494G>T	ENSP00000506339.1:p.Gly165Val
ENST00000333213.10:c.494G>T	ENSP00000327487.6:p.Gly165Val
ENST00000434205.7:c.191G>T	ENSP00000406559.3:p.Gly64Val
ENST00000578415.1:c.454G>T
ENST00000580013.5:n.511G>T
ENST00000583173.5:c.329G>T	ENSP00000463619.1:p.Gly110Val
ENST00000583818.1:c.389G>T	ENSP00000461928.1:p.Gly130Val
NM_207346.2:c.494G>T	NP_997229.2:p.Gly165Val
XM_005257229.2:c.494G>T	XP_005257286.1:p.Gly165Val
XM_006721821.2:c.191G>T	XP_006721884.1:p.Gly64Val
XM_011524616.1:c.494G>T	XP_011522918.1:p.Gly165Val
XM_011524617.1:c.494G>T	XP_011522919.1:p.Gly165Val
XM_011524618.1:c.494G>T	XP_011522920.1:p.Gly165Val
XR_243646.2:n.524G>T
XM_005257229.4:c.494G>T	XP_005257286.1:p.Gly165Val
XR_243646.4:n.530G>T
NM_207346.3:c.494G>T MANE Select	NP_997229.2:p.Gly165Val