Canonical Allele Identifier: CA2740093911

Gene: TSEN54

Linked Data

• ClinVar Variation Id: 3021617
• ClinVar RCV Id: RCV003880200

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521390C>G , CM000679.2:g.75521390C>G	GRCh38
NC_000017.10:g.73517471C>G , CM000679.1:g.73517471C>G	GRCh37
NC_000017.9:g.71029066C>G	NCBI36
NG_013041.1:g.9863C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.522-19C>G MANE Select	ENSP00000327487.6:n.522-19C>G
ENST00000434205.8:c.219-19C>G	ENSP00000406559.4:n.219-19C>G
ENST00000545228.3:c.522-19C>G	ENSP00000438169.3:n.522-19C>G
ENST00000579449.2:n.321-19C>G
ENST00000580013.6:n.531-19C>G
ENST00000583818.2:c.557C>G	ENSP00000461928.2:n.557C>G
ENST00000679370.1:n.909-19C>G
ENST00000679429.1:c.514-19C>G	ENSP00000505403.1:n.514-19C>G
ENST00000679443.1:n.397-19C>G
ENST00000679782.1:c.522-19C>G	ENSP00000505995.1:n.522-19C>G
ENST00000679919.1:n.397-19C>G
ENST00000679928.1:c.*133-19C>G	ENSP00000506071.1:n.*133-19C>G
ENST00000680528.1:n.547-19C>G
ENST00000680999.1:c.522-19C>G	ENSP00000504984.1:n.522-19C>G
ENST00000681282.1:c.522-19C>G	ENSP00000506339.1:n.522-19C>G
ENST00000333213.10:c.522-19C>G	ENSP00000327487.6:n.522-19C>G
ENST00000578415.1:c.482-19C>G
ENST00000580013.5:n.539-19C>G
ENST00000583173.5:c.357-19C>G	ENSP00000463619.1:n.357-19C>G
ENST00000583818.1:c.452C>G	ENSP00000461928.1:n.452C>G
NM_207346.2:c.522-19C>G	NP_997229.2:n.522-19C>G
XM_005257229.2:c.522-19C>G	XP_005257286.1:n.522-19C>G
XM_006721821.2:c.219-19C>G	XP_006721884.1:n.219-19C>G
XM_011524616.1:c.522-19C>G	XP_011522918.1:n.522-19C>G
XM_011524617.1:c.522-19C>G	XP_011522919.1:n.522-19C>G
XM_011524618.1:c.522-19C>G	XP_011522920.1:n.522-19C>G
XR_243646.2:n.552-19C>G
XM_005257229.4:c.522-19C>G	XP_005257286.1:n.522-19C>G
XR_243646.4:n.558-19C>G
NM_207346.3:c.522-19C>G MANE Select	NP_997229.2:n.522-19C>G