Canonical Allele Identifier: CA502045648

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517496C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521415C>G , CM000679.2:g.75521415C>G	GRCh38
NC_000017.10:g.73517496C>G , CM000679.1:g.73517496C>G	GRCh37
NC_000017.9:g.71029091C>G	NCBI36
NG_013041.1:g.9888C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.528C>G MANE Select	ENSP00000327487.6:p.Val176=
ENST00000434205.8:c.225C>G	ENSP00000406559.4:p.Val75=
ENST00000545228.3:c.528C>G	ENSP00000438169.3:p.Val176=
ENST00000579449.2:n.327C>G
ENST00000580013.6:n.537C>G
ENST00000583818.2:c.582C>G	ENSP00000461928.2:n.582C>G
ENST00000679370.1:n.915C>G
ENST00000679429.1:c.520C>G	ENSP00000505403.1:p.Pro174Ala
ENST00000679443.1:n.403C>G
ENST00000679782.1:c.528C>G	ENSP00000505995.1:p.Val176=
ENST00000679919.1:n.403C>G
ENST00000679928.1:c.*139C>G	ENSP00000506071.1:n.*139C>G
ENST00000680528.1:n.553C>G
ENST00000680999.1:c.528C>G	ENSP00000504984.1:p.Val176=
ENST00000681282.1:c.528C>G	ENSP00000506339.1:p.Val176=
ENST00000333213.10:c.528C>G	ENSP00000327487.6:p.Val176=
ENST00000578415.1:c.488C>G
ENST00000580013.5:n.545C>G
ENST00000583173.5:c.363C>G	ENSP00000463619.1:p.Val121=
ENST00000583818.1:c.477C>G	ENSP00000461928.1:n.477C>G
NM_207346.2:c.528C>G	NP_997229.2:p.Val176=
XM_005257229.2:c.528C>G	XP_005257286.1:p.Val176=
XM_006721821.2:c.225C>G	XP_006721884.1:p.Val75=
XM_011524616.1:c.528C>G	XP_011522918.1:p.Val176=
XM_011524617.1:c.528C>G	XP_011522919.1:p.Val176=
XM_011524618.1:c.528C>G	XP_011522920.1:p.Val176=
XR_243646.2:n.558C>G
XM_005257229.4:c.528C>G	XP_005257286.1:p.Val176=
XR_243646.4:n.564C>G
NM_207346.3:c.528C>G MANE Select	NP_997229.2:p.Val176=