Canonical Allele Identifier: CA2733932904

Gene: TSEN54

Linked Data

• dbSNP Id: rs764509322

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75519054C>G , CM000679.2:g.75519054C>G	GRCh38
NC_000017.10:g.73515135C>G , CM000679.1:g.73515135C>G	GRCh37
NC_000017.9:g.71026730C>G	NCBI36
NG_013041.1:g.7527C>G
NG_033152.1:g.1530G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.521+7C>G MANE Select	ENSP00000327487.6:n.521+7C>G
ENST00000434205.8:c.218+7C>G	ENSP00000406559.4:n.218+7C>G
ENST00000545228.3:c.521+7C>G	ENSP00000438169.3:n.521+7C>G
ENST00000579449.2:n.320+7C>G
ENST00000580013.6:n.530+7C>G
ENST00000583818.2:c.521+7C>G	ENSP00000461928.2:n.521+7C>G
ENST00000679370.1:n.908+7C>G
ENST00000679429.1:c.513+7C>G	ENSP00000505403.1:n.513+7C>G
ENST00000679443.1:n.396+7C>G
ENST00000679782.1:c.521+7C>G	ENSP00000505995.1:n.521+7C>G
ENST00000679919.1:n.396+7C>G
ENST00000679928.1:c.521+7C>G	ENSP00000506071.1:n.521+7C>G
ENST00000680528.1:n.546+7C>G
ENST00000680999.1:c.521+7C>G	ENSP00000504984.1:n.521+7C>G
ENST00000681282.1:c.521+7C>G	ENSP00000506339.1:n.521+7C>G
ENST00000333213.10:c.521+7C>G	ENSP00000327487.6:n.521+7C>G
ENST00000578415.1:c.481+7C>G
ENST00000580013.5:n.538+7C>G
ENST00000583173.5:c.356+7C>G	ENSP00000463619.1:n.356+7C>G
ENST00000583818.1:c.416+7C>G	ENSP00000461928.1:n.416+7C>G
NM_207346.2:c.521+7C>G	NP_997229.2:n.521+7C>G
XM_005257229.2:c.521+7C>G	XP_005257286.1:n.521+7C>G
XM_006721821.2:c.218+7C>G	XP_006721884.1:n.218+7C>G
XM_011524616.1:c.521+7C>G	XP_011522918.1:n.521+7C>G
XM_011524617.1:c.521+7C>G	XP_011522919.1:n.521+7C>G
XM_011524618.1:c.521+7C>G	XP_011522920.1:n.521+7C>G
XR_243646.2:n.551+7C>G
XM_005257229.4:c.521+7C>G	XP_005257286.1:n.521+7C>G
XR_243646.4:n.557+7C>G
NM_207346.3:c.521+7C>G MANE Select	NP_997229.2:n.521+7C>G