Canonical Allele Identifier: CA401028506

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517809C>T (hg19) ; chr17:g.75521728C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521728C>T , CM000679.2:g.75521728C>T	GRCh38
NC_000017.10:g.73517809C>T , CM000679.1:g.73517809C>T	GRCh37
NC_000017.9:g.71029404C>T	NCBI36
NG_013041.1:g.10201C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.647C>T MANE Select	ENSP00000327487.6:p.Ala216Val
ENST00000434205.8:c.344C>T	ENSP00000406559.4:p.Ala115Val
ENST00000545228.3:c.647C>T	ENSP00000438169.3:p.Ala216Val
ENST00000579449.2:n.446C>T
ENST00000580013.6:n.850C>T
ENST00000583818.2:c.701C>T	ENSP00000461928.2:n.701C>T
ENST00000679370.1:n.1228C>T
ENST00000679429.1:c.*105C>T	ENSP00000505403.1:n.*105C>T
ENST00000679443.1:n.716C>T
ENST00000679782.1:c.647C>T	ENSP00000505995.1:p.Ala216Val
ENST00000679919.1:n.716C>T
ENST00000679928.1:c.*258C>T	ENSP00000506071.1:n.*258C>T
ENST00000680528.1:n.672C>T
ENST00000680999.1:c.647C>T	ENSP00000504984.1:p.Ala216Val
ENST00000681282.1:c.676C>T	ENSP00000506339.1:p.Pro226Ser
ENST00000333213.10:c.647C>T	ENSP00000327487.6:p.Ala216Val
ENST00000578415.1:c.607C>T
ENST00000583173.5:c.458+218C>T	ENSP00000463619.1:n.458+218C>T
ENST00000583818.1:c.596C>T	ENSP00000461928.1:n.596C>T
NM_207346.2:c.647C>T	NP_997229.2:p.Ala216Val
XM_005257229.2:c.647C>T	XP_005257286.1:p.Ala216Val
XM_006721821.2:c.344C>T	XP_006721884.1:p.Ala115Val
XM_011524616.1:c.647C>T	XP_011522918.1:p.Ala216Val
XM_011524617.1:c.647C>T	XP_011522919.1:p.Ala216Val
XM_011524618.1:c.647C>T	XP_011522920.1:p.Ala216Val
XR_243646.2:n.677C>T
XM_005257229.4:c.647C>T	XP_005257286.1:p.Ala216Val
XR_243646.4:n.683C>T
NM_207346.3:c.647C>T MANE Select	NP_997229.2:p.Ala216Val