Canonical Allele Identifier: CA775072628

Gene: TSEN54

Linked Data

• dbSNP Id: rs1418067846
• gnomAD v3: 17-75516540-G-A
• gnomAD v4: 17-75516540-G-A
• MyVariant Identifiers: chr17:g.73512621G>A (hg19) ; chr17:g.75516540G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516540G>A , CM000679.2:g.75516540G>A	GRCh38
NC_000017.10:g.73512621G>A , CM000679.1:g.73512621G>A	GRCh37
NC_000017.9:g.71024216G>A	NCBI36
NG_013041.1:g.5013G>A
NG_033152.1:g.4044C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.-21G>A MANE Select	ENSP00000327487.6:n.-21G>A
ENST00000434205.8:c.-83+154G>A	ENSP00000406559.4:n.-83+154G>A
ENST00000679370.1:n.443+154G>A
ENST00000679429.1:c.-21G>A	ENSP00000505403.1:n.-21G>A
ENST00000679928.1:c.-21G>A	ENSP00000506071.1:n.-21G>A
ENST00000680528.1:n.5G>A
ENST00000681282.1:c.-21G>A	ENSP00000506339.1:n.-21G>A
ENST00000333213.10:c.-21G>A	ENSP00000327487.6:n.-21G>A
ENST00000434205.7:c.-83+154G>A	ENSP00000406559.3:n.-83+154G>A
ENST00000580013.5:n.5G>A
ENST00000583454.1:n.15G>A
NM_207346.2:c.-21G>A	NP_997229.2:n.-21G>A
XM_005257229.2:c.-21G>A	XP_005257286.1:n.-21G>A
XM_006721821.2:c.-248+154G>A	XP_006721884.1:n.-248+154G>A
XM_011524616.1:c.-21G>A	XP_011522918.1:n.-21G>A
XM_011524617.1:c.-21G>A	XP_011522919.1:n.-21G>A
XM_011524618.1:c.-21G>A	XP_011522920.1:n.-21G>A
XR_243646.2:n.10G>A
XM_005257229.4:c.-21G>A	XP_005257286.1:n.-21G>A
XR_243646.4:n.16G>A
NM_207346.3:c.-21G>A MANE Select	NP_997229.2:n.-21G>A