Canonical Allele Identifier: CA2576388780

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516540_75516541insAG , CM000679.2:g.75516540_75516541insAG	GRCh38
NC_000017.10:g.73512621_73512622insAG , CM000679.1:g.73512621_73512622insAG	GRCh37
NC_000017.9:g.71024216_71024217insAG	NCBI36
NG_013041.1:g.5013_5014insAG
NG_033152.1:g.4044_4045insTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.-21_-20insAG MANE Select	ENSP00000327487.6:n.-21_-20insAG
ENST00000434205.8:c.-83+154_-83+155insAG	ENSP00000406559.4:n.-83+154_-83+155insAG
ENST00000679370.1:n.443+154_443+155insAG
ENST00000679429.1:c.-21_-20insAG	ENSP00000505403.1:n.-21_-20insAG
ENST00000679928.1:c.-21_-20insAG	ENSP00000506071.1:n.-21_-20insAG
ENST00000680528.1:n.5_6insAG
ENST00000681282.1:c.-21_-20insAG	ENSP00000506339.1:n.-21_-20insAG
ENST00000333213.10:c.-21_-20insAG	ENSP00000327487.6:n.-21_-20insAG
ENST00000434205.7:c.-83+154_-83+155insAG	ENSP00000406559.3:n.-83+154_-83+155insAG
ENST00000580013.5:n.5_6insAG
ENST00000583454.1:n.15_16insAG
NM_207346.2:c.-21_-20insAG	NP_997229.2:n.-21_-20insAG
XM_005257229.2:c.-21_-20insAG	XP_005257286.1:n.-21_-20insAG
XM_006721821.2:c.-248+154_-248+155insAG	XP_006721884.1:n.-248+154_-248+155insAG
XM_011524616.1:c.-21_-20insAG	XP_011522918.1:n.-21_-20insAG
XM_011524617.1:c.-21_-20insAG	XP_011522919.1:n.-21_-20insAG
XM_011524618.1:c.-21_-20insAG	XP_011522920.1:n.-21_-20insAG
XR_243646.2:n.10_11insAG
XM_005257229.4:c.-21_-20insAG	XP_005257286.1:n.-21_-20insAG
XR_243646.4:n.16_17insAG
NM_207346.3:c.-21_-20insAG MANE Select	NP_997229.2:n.-21_-20insAG