Canonical Allele Identifier: CA401026838

Gene: TSEN54

Linked Data

• dbSNP Id: rs1256038429
• gnomAD v2: 17-73512667-C-A
• gnomAD v4: 17-75516586-C-A
• MyVariant Identifiers: chr17:g.73512667C>A (hg19) ; chr17:g.75516586C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516586C>A , CM000679.2:g.75516586C>A	GRCh38
NC_000017.10:g.73512667C>A , CM000679.1:g.73512667C>A	GRCh37
NC_000017.9:g.71024262C>A	NCBI36
NG_013041.1:g.5059C>A
NG_033152.1:g.3998G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.26C>A MANE Select	ENSP00000327487.6:p.Ala9Asp
ENST00000434205.8:c.-83+200C>A	ENSP00000406559.4:n.-83+200C>A
ENST00000545228.3:c.26C>A	ENSP00000438169.3:p.Ala9Asp
ENST00000580013.6:n.35C>A
ENST00000583818.2:c.26C>A	ENSP00000461928.2:p.Ala9Asp
ENST00000679370.1:n.444-160C>A
ENST00000679429.1:c.26C>A	ENSP00000505403.1:p.Ala9Asp
ENST00000679782.1:c.26C>A	ENSP00000505995.1:p.Ala9Asp
ENST00000679928.1:c.26C>A	ENSP00000506071.1:p.Ala9Asp
ENST00000680528.1:n.51C>A
ENST00000680999.1:c.26C>A	ENSP00000504984.1:p.Ala9Asp
ENST00000681282.1:c.26C>A	ENSP00000506339.1:p.Ala9Asp
ENST00000333213.10:c.26C>A	ENSP00000327487.6:p.Ala9Asp
ENST00000434205.7:c.-83+200C>A	ENSP00000406559.3:n.-83+200C>A
ENST00000580013.5:n.51C>A
ENST00000583173.5:c.26C>A	ENSP00000463619.1:p.Ala9Asp
ENST00000583454.1:n.61C>A
NM_207346.2:c.26C>A	NP_997229.2:p.Ala9Asp
XM_005257229.2:c.26C>A	XP_005257286.1:p.Ala9Asp
XM_006721821.2:c.-247-160C>A	XP_006721884.1:n.-247-160C>A
XM_011524616.1:c.26C>A	XP_011522918.1:p.Ala9Asp
XM_011524617.1:c.26C>A	XP_011522919.1:p.Ala9Asp
XM_011524618.1:c.26C>A	XP_011522920.1:p.Ala9Asp
XR_243646.2:n.56C>A
XM_005257229.4:c.26C>A	XP_005257286.1:p.Ala9Asp
XR_243646.4:n.62C>A
NM_207346.3:c.26C>A MANE Select	NP_997229.2:p.Ala9Asp