Canonical Allele Identifier: CA502046151

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517951C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521870C>G , CM000679.2:g.75521870C>G	GRCh38
NC_000017.10:g.73517951C>G , CM000679.1:g.73517951C>G	GRCh37
NC_000017.9:g.71029546C>G	NCBI36
NG_013041.1:g.10343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.789C>G MANE Select	ENSP00000327487.6:p.Ser263=
ENST00000434205.8:c.486C>G	ENSP00000406559.4:p.Ser162=
ENST00000545228.3:c.789C>G	ENSP00000438169.3:p.Ser263=
ENST00000579449.2:n.588C>G
ENST00000580013.6:n.992C>G
ENST00000583818.2:c.843C>G	ENSP00000461928.2:n.843C>G
ENST00000679370.1:n.1370C>G
ENST00000679429.1:c.*247C>G	ENSP00000505403.1:n.*247C>G
ENST00000679443.1:n.858C>G
ENST00000679782.1:c.789C>G	ENSP00000505995.1:p.Ser263=
ENST00000679919.1:n.858C>G
ENST00000679928.1:c.*400C>G	ENSP00000506071.1:n.*400C>G
ENST00000680528.1:n.814C>G
ENST00000680999.1:c.789C>G	ENSP00000504984.1:p.Ser263=
ENST00000681282.1:c.*35C>G	ENSP00000506339.1:n.*35C>G
ENST00000333213.10:c.789C>G	ENSP00000327487.6:p.Ser263=
ENST00000578415.1:c.749C>G
ENST00000583173.5:c.459-137C>G	ENSP00000463619.1:n.459-137C>G
ENST00000583818.1:c.738C>G	ENSP00000461928.1:n.738C>G
NM_207346.2:c.789C>G	NP_997229.2:p.Ser263=
XM_005257229.2:c.789C>G	XP_005257286.1:p.Ser263=
XM_006721821.2:c.486C>G	XP_006721884.1:p.Ser162=
XM_011524616.1:c.789C>G	XP_011522918.1:p.Ser263=
XM_011524617.1:c.789C>G	XP_011522919.1:p.Ser263=
XM_011524618.1:c.789C>G	XP_011522920.1:p.Ser263=
XR_243646.2:n.819C>G
XM_005257229.4:c.789C>G	XP_005257286.1:p.Ser263=
XR_243646.4:n.825C>G
NM_207346.3:c.789C>G MANE Select	NP_997229.2:p.Ser263=