Canonical Allele Identifier: CA627406570

Gene: TSEN54

Linked Data

• dbSNP Id: rs1460544470
• gnomAD v2: 17-73520161-T-TC
• gnomAD v3: 17-75524080-T-TC
• gnomAD v4: 17-75524080-T-TC
• MyVariant Identifiers: chr17:g.73520161_73520162insC (hg19) ; chr17:g.75524080_75524081insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524082dup , CM000679.2:g.75524082dup	GRCh38
NC_000017.10:g.73520163dup , CM000679.1:g.73520163dup	GRCh37
NC_000017.9:g.71031758dup	NCBI36
NG_013041.1:g.12555dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1431-180dup MANE Select	ENSP00000327487.6:n.1431-180dup
ENST00000434205.8:c.1128-180dup	ENSP00000406559.4:n.1128-180dup
ENST00000545228.3:c.1619-180dup	ENSP00000438169.3:n.1619-180dup
ENST00000577197.2:n.629-180dup
ENST00000579449.2:n.2171-180dup
ENST00000580013.6:n.2575-180dup
ENST00000679370.1:n.2953-180dup
ENST00000679429.1:c.*889-180dup	ENSP00000505403.1:n.*889-180dup
ENST00000679443.1:n.1500-180dup
ENST00000679782.1:c.*130-180dup	ENSP00000505995.1:n.*130-180dup
ENST00000679919.1:n.1702-180dup
ENST00000679928.1:c.*1983-180dup	ENSP00000506071.1:n.*1983-180dup
ENST00000680528.1:n.2397-180dup
ENST00000680999.1:c.1644-180dup	ENSP00000504984.1:n.1644-180dup
ENST00000681282.1:c.*1618-180dup	ENSP00000506339.1:n.*1618-180dup
ENST00000333213.10:c.1431-180dup	ENSP00000327487.6:n.1431-180dup
ENST00000545228.2:c.708-180dup
ENST00000577197.1:n.179-180dup
ENST00000579449.1:n.628-180dup
NM_207346.2:c.1431-180dup	NP_997229.2:n.1431-180dup
XM_005257229.2:c.1619-180dup	XP_005257286.1:n.1619-180dup
XM_006721821.2:c.1316-180dup	XP_006721884.1:n.1316-180dup
XM_011524616.1:c.1502-180dup	XP_011522918.1:n.1502-180dup
XM_011524617.1:c.*13-180dup	XP_011522919.1:n.*13-180dup
XM_011524618.1:c.1314-180dup	XP_011522920.1:n.1314-180dup
XR_243646.2:n.1663-180dup
XM_005257229.4:c.1619-180dup	XP_005257286.1:n.1619-180dup
XR_001753015.1:n.87+230dup
XR_001753016.1:n.88+230dup
XR_243646.4:n.1669-180dup
NM_207346.3:c.1431-180dup MANE Select	NP_997229.2:n.1431-180dup