Canonical Allele Identifier: CA2275548438

Gene: TSEN54

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516738_75516739delinsTC , CM000679.2:g.75516738_75516739delinsTC	GRCh38
NC_000017.10:g.73512819_73512820delinsTC , CM000679.1:g.73512819_73512820delinsTC	GRCh37
NC_000017.9:g.71024414_71024415delinsTC	NCBI36
NG_013041.1:g.5211_5212delinsTC
NG_033152.1:g.3845_3846delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.57-8_57-7delinsTC MANE Select	ENSP00000327487.6:n.57-8_57-7delinsTC
ENST00000434205.8:c.-82-271_-82-270delinsTC	ENSP00000406559.4:n.-82-271_-82-270delinsTC
ENST00000545228.3:c.57-8_57-7delinsTC	ENSP00000438169.3:n.57-8_57-7delinsTC
ENST00000579449.2:n.20+122_20+123delinsTC
ENST00000580013.6:n.66-8_66-7delinsTC
ENST00000583818.2:c.57-8_57-7delinsTC	ENSP00000461928.2:n.57-8_57-7delinsTC
ENST00000679370.1:n.444-8_444-7delinsTC
ENST00000679429.1:c.57-8_57-7delinsTC	ENSP00000505403.1:n.57-8_57-7delinsTC
ENST00000679782.1:c.57-8_57-7delinsTC	ENSP00000505995.1:n.57-8_57-7delinsTC
ENST00000679928.1:c.57-8_57-7delinsTC	ENSP00000506071.1:n.57-8_57-7delinsTC
ENST00000680528.1:n.82-8_82-7delinsTC
ENST00000680999.1:c.57-8_57-7delinsTC	ENSP00000504984.1:n.57-8_57-7delinsTC
ENST00000681282.1:c.57-8_57-7delinsTC	ENSP00000506339.1:n.57-8_57-7delinsTC
ENST00000333213.10:c.57-8_57-7delinsTC	ENSP00000327487.6:n.57-8_57-7delinsTC
ENST00000434205.7:c.-82-271_-82-270delinsTC	ENSP00000406559.3:n.-82-271_-82-270delinsTC
ENST00000580013.5:n.82-8_82-7delinsTC
ENST00000583173.5:c.56+122_56+123delinsTC	ENSP00000463619.1:n.56+122_56+123delinsTC
ENST00000583454.1:n.92-8_92-7delinsTC
NM_207346.2:c.57-8_57-7delinsTC	NP_997229.2:n.57-8_57-7delinsTC
XM_005257229.2:c.57-8_57-7delinsTC	XP_005257286.1:n.57-8_57-7delinsTC
XM_006721821.2:c.-247-8_-247-7delinsTC	XP_006721884.1:n.-247-8_-247-7delinsTC
XM_011524616.1:c.57-8_57-7delinsTC	XP_011522918.1:n.57-8_57-7delinsTC
XM_011524617.1:c.57-8_57-7delinsTC	XP_011522919.1:n.57-8_57-7delinsTC
XM_011524618.1:c.57-8_57-7delinsTC	XP_011522920.1:n.57-8_57-7delinsTC
XR_243646.2:n.87-8_87-7delinsTC
XM_005257229.4:c.57-8_57-7delinsTC	XP_005257286.1:n.57-8_57-7delinsTC
XR_243646.4:n.93-8_93-7delinsTC
NM_207346.3:c.57-8_57-7delinsTC MANE Select	NP_997229.2:n.57-8_57-7delinsTC