Canonical Allele Identifier: CA775074870

Gene: TSEN54

Linked Data

• dbSNP Id: rs1279202045
• MyVariant Identifiers: chr17:g.73514962_73514963del (hg19) ; chr17:g.75518881_75518882del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75518881_75518882del , CM000679.2:g.75518881_75518882del	GRCh38
NC_000017.10:g.73514962_73514963del , CM000679.1:g.73514962_73514963del	GRCh37
NC_000017.9:g.71026557_71026558del	NCBI36
NG_013041.1:g.7354_7355del
NG_033152.1:g.1702_1703del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.469-114_469-113del MANE Select	ENSP00000327487.6:n.469-114_469-113del
ENST00000434205.8:c.166-114_166-113del	ENSP00000406559.4:n.166-114_166-113del
ENST00000545228.3:c.469-114_469-113del	ENSP00000438169.3:n.469-114_469-113del
ENST00000579449.2:n.268-114_268-113del
ENST00000580013.6:n.478-114_478-113del
ENST00000583818.2:c.469-114_469-113del	ENSP00000461928.2:n.469-114_469-113del
ENST00000679370.1:n.856-114_856-113del
ENST00000679429.1:c.469-122_469-121del	ENSP00000505403.1:n.469-122_469-121del
ENST00000679443.1:n.344-114_344-113del
ENST00000679782.1:c.469-114_469-113del	ENSP00000505995.1:n.469-114_469-113del
ENST00000679919.1:n.344-114_344-113del
ENST00000679928.1:c.469-114_469-113del	ENSP00000506071.1:n.469-114_469-113del
ENST00000680528.1:n.494-114_494-113del
ENST00000680999.1:c.469-114_469-113del	ENSP00000504984.1:n.469-114_469-113del
ENST00000681282.1:c.469-114_469-113del	ENSP00000506339.1:n.469-114_469-113del
ENST00000333213.10:c.469-114_469-113del	ENSP00000327487.6:n.469-114_469-113del
ENST00000434205.7:c.166-114_166-113del	ENSP00000406559.3:n.166-114_166-113del
ENST00000578415.1:c.429-114_429-113del
ENST00000580013.5:n.494-122_494-121del
ENST00000583173.5:c.304-114_304-113del	ENSP00000463619.1:n.304-114_304-113del
ENST00000583818.1:c.364-114_364-113del	ENSP00000461928.1:n.364-114_364-113del
NM_207346.2:c.469-114_469-113del	NP_997229.2:n.469-114_469-113del
XM_005257229.2:c.469-114_469-113del	XP_005257286.1:n.469-114_469-113del
XM_006721821.2:c.166-114_166-113del	XP_006721884.1:n.166-114_166-113del
XM_011524616.1:c.469-114_469-113del	XP_011522918.1:n.469-114_469-113del
XM_011524617.1:c.469-114_469-113del	XP_011522919.1:n.469-114_469-113del
XM_011524618.1:c.469-114_469-113del	XP_011522920.1:n.469-114_469-113del
XR_243646.2:n.499-114_499-113del
XM_005257229.4:c.469-114_469-113del	XP_005257286.1:n.469-114_469-113del
XR_243646.4:n.505-114_505-113del
NM_207346.3:c.469-114_469-113del MANE Select	NP_997229.2:n.469-114_469-113del