Canonical Allele Identifier: CA401029222

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75521925-G-A
• MyVariant Identifiers: chr17:g.73518006G>A (hg19) ; chr17:g.75521925G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521925G>A , CM000679.2:g.75521925G>A	GRCh38
NC_000017.10:g.73518006G>A , CM000679.1:g.73518006G>A	GRCh37
NC_000017.9:g.71029601G>A	NCBI36
NG_013041.1:g.10398G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.844G>A MANE Select	ENSP00000327487.6:p.Gly282Ser
ENST00000434205.8:c.541G>A	ENSP00000406559.4:p.Gly181Ser
ENST00000545228.3:c.844G>A	ENSP00000438169.3:p.Gly282Ser
ENST00000579449.2:n.643G>A
ENST00000580013.6:n.1047G>A
ENST00000679370.1:n.1425G>A
ENST00000679429.1:c.*302G>A	ENSP00000505403.1:n.*302G>A
ENST00000679443.1:n.913G>A
ENST00000679782.1:c.844G>A	ENSP00000505995.1:p.Gly282Ser
ENST00000679919.1:n.913G>A
ENST00000679928.1:c.*455G>A	ENSP00000506071.1:n.*455G>A
ENST00000680528.1:n.869G>A
ENST00000680999.1:c.844G>A	ENSP00000504984.1:p.Gly282Ser
ENST00000681282.1:c.*90G>A	ENSP00000506339.1:n.*90G>A
ENST00000333213.10:c.844G>A	ENSP00000327487.6:p.Gly282Ser
ENST00000578415.1:c.804G>A
ENST00000583173.5:c.459-82G>A	ENSP00000463619.1:n.459-82G>A
NM_207346.2:c.844G>A	NP_997229.2:p.Gly282Ser
XM_005257229.2:c.844G>A	XP_005257286.1:p.Gly282Ser
XM_006721821.2:c.541G>A	XP_006721884.1:p.Gly181Ser
XM_011524616.1:c.844G>A	XP_011522918.1:p.Gly282Ser
XM_011524617.1:c.844G>A	XP_011522919.1:p.Gly282Ser
XM_011524618.1:c.844G>A	XP_011522920.1:p.Gly282Ser
XR_243646.2:n.874G>A
XM_005257229.4:c.844G>A	XP_005257286.1:p.Gly282Ser
XR_243646.4:n.880G>A
NM_207346.3:c.844G>A MANE Select	NP_997229.2:p.Gly282Ser