Canonical Allele Identifier: CA294079311

Gene: TSEN54

Linked Data

• dbSNP Id: rs867700810
• gnomAD v4: 17-75522102-C-A
• MyVariant Identifiers: chr17:g.73518183C>A (hg19) ; chr17:g.75522102C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522102C>A , CM000679.2:g.75522102C>A	GRCh38
NC_000017.10:g.73518183C>A , CM000679.1:g.73518183C>A	GRCh37
NC_000017.9:g.71029778C>A	NCBI36
NG_013041.1:g.10575C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1021C>A MANE Select	ENSP00000327487.6:p.Leu341Met
ENST00000434205.8:c.718C>A	ENSP00000406559.4:p.Leu240Met
ENST00000545228.3:c.1021C>A	ENSP00000438169.3:p.Leu341Met
ENST00000579449.2:n.820C>A
ENST00000580013.6:n.1224C>A
ENST00000679370.1:n.1602C>A
ENST00000679429.1:c.*479C>A	ENSP00000505403.1:n.*479C>A
ENST00000679443.1:n.1090C>A
ENST00000679782.1:c.1021C>A	ENSP00000505995.1:p.Leu341Met
ENST00000679919.1:n.1090C>A
ENST00000679928.1:c.*632C>A	ENSP00000506071.1:n.*632C>A
ENST00000680528.1:n.1046C>A
ENST00000680999.1:c.1021C>A	ENSP00000504984.1:p.Leu341Met
ENST00000681282.1:c.*267C>A	ENSP00000506339.1:n.*267C>A
ENST00000333213.10:c.1021C>A	ENSP00000327487.6:p.Leu341Met
ENST00000545228.2:c.110C>A
ENST00000578415.1:c.981C>A
ENST00000583173.5:c.554C>A	ENSP00000463619.1:n.554C>A
NM_207346.2:c.1021C>A	NP_997229.2:p.Leu341Met
XM_005257229.2:c.1021C>A	XP_005257286.1:p.Leu341Met
XM_006721821.2:c.718C>A	XP_006721884.1:p.Leu240Met
XM_011524616.1:c.1021C>A	XP_011522918.1:p.Leu341Met
XM_011524617.1:c.1021C>A	XP_011522919.1:p.Leu341Met
XM_011524618.1:c.1021C>A	XP_011522920.1:p.Leu341Met
XR_243646.2:n.1051C>A
XM_005257229.4:c.1021C>A	XP_005257286.1:p.Leu341Met
XR_243646.4:n.1057C>A
NM_207346.3:c.1021C>A MANE Select	NP_997229.2:p.Leu341Met