Canonical Allele Identifier: CA775072623

Gene: TSEN54

Linked Data

• dbSNP Id: rs1411991502
• MyVariant Identifiers: chr17:g.73512620del (hg19) ; chr17:g.75516539del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516539del , CM000679.2:g.75516539del	GRCh38
NC_000017.10:g.73512620del , CM000679.1:g.73512620del	GRCh37
NC_000017.9:g.71024215del	NCBI36
NG_013041.1:g.5012del
NG_033152.1:g.4045del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.-22del MANE Select	ENSP00000327487.6:n.-22del
ENST00000434205.8:c.-83+153del	ENSP00000406559.4:n.-83+153del
ENST00000679370.1:n.443+153del
ENST00000679429.1:c.-22del	ENSP00000505403.1:n.-22del
ENST00000679928.1:c.-22del	ENSP00000506071.1:n.-22del
ENST00000680528.1:n.4del
ENST00000681282.1:c.-22del	ENSP00000506339.1:n.-22del
ENST00000333213.10:c.-22del	ENSP00000327487.6:n.-22del
ENST00000434205.7:c.-83+153del	ENSP00000406559.3:n.-83+153del
ENST00000580013.5:n.4del
ENST00000583454.1:n.14del
NM_207346.2:c.-22del	NP_997229.2:n.-22del
XM_005257229.2:c.-22del	XP_005257286.1:n.-22del
XM_006721821.2:c.-248+153del	XP_006721884.1:n.-248+153del
XM_011524616.1:c.-22del	XP_011522918.1:n.-22del
XM_011524617.1:c.-22del	XP_011522919.1:n.-22del
XM_011524618.1:c.-22del	XP_011522920.1:n.-22del
XR_243646.2:n.9del
XM_005257229.4:c.-22del	XP_005257286.1:n.-22del
XR_243646.4:n.15del
NM_207346.3:c.-22del MANE Select	NP_997229.2:n.-22del