Canonical Allele Identifier: CA627405790

Gene: TSEN54

Linked Data

• dbSNP Id: rs1215066871
• gnomAD v2: 17-73512757-ACCGGCGC-A
• gnomAD v3: 17-75516676-ACCGGCGC-A
• gnomAD v4: 17-75516676-ACCGGCGC-A
• MyVariant Identifiers: chr17:g.73512758_73512764del (hg19) ; chr17:g.75516677_75516683del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516681_75516687del , CM000679.2:g.75516681_75516687del	GRCh38
NC_000017.10:g.73512762_73512768del , CM000679.1:g.73512762_73512768del	GRCh37
NC_000017.9:g.71024357_71024363del	NCBI36
NG_013041.1:g.5154_5160del
NG_033152.1:g.3901_3907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.57-65_57-59del MANE Select	ENSP00000327487.6:n.57-65_57-59del
ENST00000434205.8:c.-83+295_-83+301del	ENSP00000406559.4:n.-83+295_-83+301del
ENST00000545228.3:c.57-65_57-59del	ENSP00000438169.3:n.57-65_57-59del
ENST00000579449.2:n.20+65_20+71del
ENST00000580013.6:n.66-65_66-59del
ENST00000583818.2:c.57-65_57-59del	ENSP00000461928.2:n.57-65_57-59del
ENST00000679370.1:n.444-65_444-59del
ENST00000679429.1:c.57-65_57-59del	ENSP00000505403.1:n.57-65_57-59del
ENST00000679782.1:c.57-65_57-59del	ENSP00000505995.1:n.57-65_57-59del
ENST00000679928.1:c.57-65_57-59del	ENSP00000506071.1:n.57-65_57-59del
ENST00000680528.1:n.82-65_82-59del
ENST00000680999.1:c.57-65_57-59del	ENSP00000504984.1:n.57-65_57-59del
ENST00000681282.1:c.57-65_57-59del	ENSP00000506339.1:n.57-65_57-59del
ENST00000333213.10:c.57-65_57-59del	ENSP00000327487.6:n.57-65_57-59del
ENST00000434205.7:c.-83+295_-83+301del	ENSP00000406559.3:n.-83+295_-83+301del
ENST00000580013.5:n.82-65_82-59del
ENST00000583173.5:c.56+65_56+71del	ENSP00000463619.1:n.56+65_56+71del
ENST00000583454.1:n.92-65_92-59del
NM_207346.2:c.57-65_57-59del	NP_997229.2:n.57-65_57-59del
XM_005257229.2:c.57-65_57-59del	XP_005257286.1:n.57-65_57-59del
XM_006721821.2:c.-247-65_-247-59del	XP_006721884.1:n.-247-65_-247-59del
XM_011524616.1:c.57-65_57-59del	XP_011522918.1:n.57-65_57-59del
XM_011524617.1:c.57-65_57-59del	XP_011522919.1:n.57-65_57-59del
XM_011524618.1:c.57-65_57-59del	XP_011522920.1:n.57-65_57-59del
XR_243646.2:n.87-65_87-59del
XM_005257229.4:c.57-65_57-59del	XP_005257286.1:n.57-65_57-59del
XR_243646.4:n.93-65_93-59del
NM_207346.3:c.57-65_57-59del MANE Select	NP_997229.2:n.57-65_57-59del