Canonical Allele Identifier: CA401029821

Gene: TSEN54

Linked Data

• dbSNP Id: rs1390982969
• gnomAD v2: 17-73518259-T-G
• gnomAD v3: 17-75522178-T-G
• gnomAD v4: 17-75522178-T-G
• MyVariant Identifiers: chr17:g.73518259T>G (hg19) ; chr17:g.75522178T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75522178T>G , CM000679.2:g.75522178T>G	GRCh38
NC_000017.10:g.73518259T>G , CM000679.1:g.73518259T>G	GRCh37
NC_000017.9:g.71029854T>G	NCBI36
NG_013041.1:g.10651T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.1097T>G MANE Select	ENSP00000327487.6:p.Val366Gly
ENST00000434205.8:c.794T>G	ENSP00000406559.4:p.Val265Gly
ENST00000545228.3:c.1097T>G	ENSP00000438169.3:p.Val366Gly
ENST00000579449.2:n.896T>G
ENST00000580013.6:n.1300T>G
ENST00000679370.1:n.1678T>G
ENST00000679429.1:c.*555T>G	ENSP00000505403.1:n.*555T>G
ENST00000679443.1:n.1166T>G
ENST00000679782.1:c.1097T>G	ENSP00000505995.1:p.Val366Gly
ENST00000679919.1:n.1166T>G
ENST00000679928.1:c.*708T>G	ENSP00000506071.1:n.*708T>G
ENST00000680528.1:n.1122T>G
ENST00000680999.1:c.1097T>G	ENSP00000504984.1:p.Val366Gly
ENST00000681282.1:c.*343T>G	ENSP00000506339.1:n.*343T>G
ENST00000333213.10:c.1097T>G	ENSP00000327487.6:p.Val366Gly
ENST00000545228.2:c.186T>G
ENST00000583173.5:c.630T>G	ENSP00000463619.1:n.630T>G
NM_207346.2:c.1097T>G	NP_997229.2:p.Val366Gly
XM_005257229.2:c.1097T>G	XP_005257286.1:p.Val366Gly
XM_006721821.2:c.794T>G	XP_006721884.1:p.Val265Gly
XM_011524616.1:c.1097T>G	XP_011522918.1:p.Val366Gly
XM_011524617.1:c.1097T>G	XP_011522919.1:p.Val366Gly
XM_011524618.1:c.1097T>G	XP_011522920.1:p.Val366Gly
XR_243646.2:n.1127T>G
XM_005257229.4:c.1097T>G	XP_005257286.1:p.Val366Gly
XR_243646.4:n.1133T>G
NM_207346.3:c.1097T>G MANE Select	NP_997229.2:p.Val366Gly