Canonical Allele Identifier: CA401026945

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75516762-G-A
• MyVariant Identifiers: chr17:g.73512843G>A (hg19) ; chr17:g.75516762G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516762G>A , CM000679.2:g.75516762G>A	GRCh38
NC_000017.10:g.73512843G>A , CM000679.1:g.73512843G>A	GRCh37
NC_000017.9:g.71024438G>A	NCBI36
NG_013041.1:g.5235G>A
NG_033152.1:g.3822C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.73G>A MANE Select	ENSP00000327487.6:p.Ala25Thr
ENST00000434205.8:c.-82-247G>A	ENSP00000406559.4:n.-82-247G>A
ENST00000545228.3:c.73G>A	ENSP00000438169.3:p.Ala25Thr
ENST00000579449.2:n.20+146G>A
ENST00000580013.6:n.82G>A
ENST00000583818.2:c.73G>A	ENSP00000461928.2:p.Ala25Thr
ENST00000679370.1:n.460G>A
ENST00000679429.1:c.73G>A	ENSP00000505403.1:p.Ala25Thr
ENST00000679782.1:c.73G>A	ENSP00000505995.1:p.Ala25Thr
ENST00000679928.1:c.73G>A	ENSP00000506071.1:p.Ala25Thr
ENST00000680528.1:n.98G>A
ENST00000680999.1:c.73G>A	ENSP00000504984.1:p.Ala25Thr
ENST00000681282.1:c.73G>A	ENSP00000506339.1:p.Ala25Thr
ENST00000333213.10:c.73G>A	ENSP00000327487.6:p.Ala25Thr
ENST00000434205.7:c.-82-247G>A	ENSP00000406559.3:n.-82-247G>A
ENST00000580013.5:n.98G>A
ENST00000583173.5:c.56+146G>A	ENSP00000463619.1:n.56+146G>A
ENST00000583454.1:n.108G>A
NM_207346.2:c.73G>A	NP_997229.2:p.Ala25Thr
XM_005257229.2:c.73G>A	XP_005257286.1:p.Ala25Thr
XM_006721821.2:c.-231G>A	XP_006721884.1:n.-231G>A
XM_011524616.1:c.73G>A	XP_011522918.1:p.Ala25Thr
XM_011524617.1:c.73G>A	XP_011522919.1:p.Ala25Thr
XM_011524618.1:c.73G>A	XP_011522920.1:p.Ala25Thr
XR_243646.2:n.103G>A
XM_005257229.4:c.73G>A	XP_005257286.1:p.Ala25Thr
XR_243646.4:n.109G>A
NM_207346.3:c.73G>A MANE Select	NP_997229.2:p.Ala25Thr