Canonical Allele Identifier: CA401029652

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73518177C>G (hg19) ; chr17:g.75522096C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522096C>G , CM000679.2:g.75522096C>G	GRCh38
NC_000017.10:g.73518177C>G , CM000679.1:g.73518177C>G	GRCh37
NC_000017.9:g.71029772C>G	NCBI36
NG_013041.1:g.10569C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1015C>G MANE Select	ENSP00000327487.6:p.Gln339Glu
ENST00000434205.8:c.712C>G	ENSP00000406559.4:p.Gln238Glu
ENST00000545228.3:c.1015C>G	ENSP00000438169.3:p.Gln339Glu
ENST00000579449.2:n.814C>G
ENST00000580013.6:n.1218C>G
ENST00000679370.1:n.1596C>G
ENST00000679429.1:c.*473C>G	ENSP00000505403.1:n.*473C>G
ENST00000679443.1:n.1084C>G
ENST00000679782.1:c.1015C>G	ENSP00000505995.1:p.Gln339Glu
ENST00000679919.1:n.1084C>G
ENST00000679928.1:c.*626C>G	ENSP00000506071.1:n.*626C>G
ENST00000680528.1:n.1040C>G
ENST00000680999.1:c.1015C>G	ENSP00000504984.1:p.Gln339Glu
ENST00000681282.1:c.*261C>G	ENSP00000506339.1:n.*261C>G
ENST00000333213.10:c.1015C>G	ENSP00000327487.6:p.Gln339Glu
ENST00000545228.2:c.104C>G
ENST00000578415.1:c.975C>G
ENST00000583173.5:c.548C>G	ENSP00000463619.1:n.548C>G
NM_207346.2:c.1015C>G	NP_997229.2:p.Gln339Glu
XM_005257229.2:c.1015C>G	XP_005257286.1:p.Gln339Glu
XM_006721821.2:c.712C>G	XP_006721884.1:p.Gln238Glu
XM_011524616.1:c.1015C>G	XP_011522918.1:p.Gln339Glu
XM_011524617.1:c.1015C>G	XP_011522919.1:p.Gln339Glu
XM_011524618.1:c.1015C>G	XP_011522920.1:p.Gln339Glu
XR_243646.2:n.1045C>G
XM_005257229.4:c.1015C>G	XP_005257286.1:p.Gln339Glu
XR_243646.4:n.1051C>G
NM_207346.3:c.1015C>G MANE Select	NP_997229.2:p.Gln339Glu