Canonical Allele Identifier: CA501819510

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73520424G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524343G>C , CM000679.2:g.75524343G>C	GRCh38
NC_000017.10:g.73520424G>C , CM000679.1:g.73520424G>C	GRCh37
NC_000017.9:g.71032019G>C	NCBI36
NG_013041.1:g.12816G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1512G>C MANE Select	ENSP00000327487.6:p.Leu504=
ENST00000434205.8:c.1209G>C	ENSP00000406559.4:p.Leu403=
ENST00000545228.3:c.*11G>C	ENSP00000438169.3:n.*11G>C
ENST00000577197.2:n.710G>C
ENST00000579449.2:n.2252G>C
ENST00000580013.6:n.2656G>C
ENST00000679370.1:n.3034G>C
ENST00000679429.1:c.*970G>C	ENSP00000505403.1:n.*970G>C
ENST00000679443.1:n.1581G>C
ENST00000679782.1:c.*211G>C	ENSP00000505995.1:n.*211G>C
ENST00000679919.1:n.1783G>C
ENST00000679928.1:c.*2064G>C	ENSP00000506071.1:n.*2064G>C
ENST00000680528.1:n.2478G>C
ENST00000680999.1:c.1725G>C	ENSP00000504984.1:p.Leu575=
ENST00000681282.1:c.*1699G>C	ENSP00000506339.1:n.*1699G>C
ENST00000333213.10:c.1512G>C	ENSP00000327487.6:p.Leu504=
ENST00000545228.2:c.789G>C
ENST00000577197.1:n.260G>C
ENST00000579449.1:n.709G>C
NM_207346.2:c.1512G>C	NP_997229.2:p.Leu504=
XM_005257229.2:c.*11G>C	XP_005257286.1:n.*11G>C
XM_006721821.2:c.*11G>C	XP_006721884.1:n.*11G>C
XM_011524616.1:c.*11G>C	XP_011522918.1:n.*11G>C
XM_011524617.1:c.*94G>C	XP_011522919.1:n.*94G>C
XM_011524618.1:c.1395G>C	XP_011522920.1:p.Leu465=
XR_243646.2:n.1744G>C
XM_005257229.4:c.*11G>C	XP_005257286.1:n.*11G>C
XR_001753015.1:n.55C>G
XR_001753016.1:n.56C>G
XR_243646.4:n.1750G>C
NM_207346.3:c.1512G>C MANE Select	NP_997229.2:p.Leu504=