Canonical Allele Identifier: CA401028690

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517859C>T (hg19) ; chr17:g.75521778C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521778C>T , CM000679.2:g.75521778C>T	GRCh38
NC_000017.10:g.73517859C>T , CM000679.1:g.73517859C>T	GRCh37
NC_000017.9:g.71029454C>T	NCBI36
NG_013041.1:g.10251C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.697C>T MANE Select	ENSP00000327487.6:p.Pro233Ser
ENST00000434205.8:c.394C>T	ENSP00000406559.4:p.Pro132Ser
ENST00000545228.3:c.697C>T	ENSP00000438169.3:p.Pro233Ser
ENST00000579449.2:n.496C>T
ENST00000580013.6:n.900C>T
ENST00000583818.2:c.751C>T	ENSP00000461928.2:n.751C>T
ENST00000679370.1:n.1278C>T
ENST00000679429.1:c.*155C>T	ENSP00000505403.1:n.*155C>T
ENST00000679443.1:n.766C>T
ENST00000679782.1:c.697C>T	ENSP00000505995.1:p.Pro233Ser
ENST00000679919.1:n.766C>T
ENST00000679928.1:c.*308C>T	ENSP00000506071.1:n.*308C>T
ENST00000680528.1:n.722C>T
ENST00000680999.1:c.697C>T	ENSP00000504984.1:p.Pro233Ser
ENST00000681282.1:c.726C>T	ENSP00000506339.1:p.Leu242=
ENST00000333213.10:c.697C>T	ENSP00000327487.6:p.Pro233Ser
ENST00000578415.1:c.657C>T
ENST00000583173.5:c.459-229C>T	ENSP00000463619.1:n.459-229C>T
ENST00000583818.1:c.646C>T	ENSP00000461928.1:n.646C>T
NM_207346.2:c.697C>T	NP_997229.2:p.Pro233Ser
XM_005257229.2:c.697C>T	XP_005257286.1:p.Pro233Ser
XM_006721821.2:c.394C>T	XP_006721884.1:p.Pro132Ser
XM_011524616.1:c.697C>T	XP_011522918.1:p.Pro233Ser
XM_011524617.1:c.697C>T	XP_011522919.1:p.Pro233Ser
XM_011524618.1:c.697C>T	XP_011522920.1:p.Pro233Ser
XR_243646.2:n.727C>T
XM_005257229.4:c.697C>T	XP_005257286.1:p.Pro233Ser
XR_243646.4:n.733C>T
NM_207346.3:c.697C>T MANE Select	NP_997229.2:p.Pro233Ser