Canonical Allele Identifier: CA401026934

Gene: TSEN54

Linked Data

• gnomAD v4: 17-75516757-T-C
• MyVariant Identifiers: chr17:g.73512838T>C (hg19) ; chr17:g.75516757T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75516757T>C , CM000679.2:g.75516757T>C	GRCh38
NC_000017.10:g.73512838T>C , CM000679.1:g.73512838T>C	GRCh37
NC_000017.9:g.71024433T>C	NCBI36
NG_013041.1:g.5230T>C
NG_033152.1:g.3827A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.68T>C MANE Select	ENSP00000327487.6:p.Leu23Pro
ENST00000434205.8:c.-82-252T>C	ENSP00000406559.4:n.-82-252T>C
ENST00000545228.3:c.68T>C	ENSP00000438169.3:p.Leu23Pro
ENST00000579449.2:n.20+141T>C
ENST00000580013.6:n.77T>C
ENST00000583818.2:c.68T>C	ENSP00000461928.2:p.Leu23Pro
ENST00000679370.1:n.455T>C
ENST00000679429.1:c.68T>C	ENSP00000505403.1:p.Leu23Pro
ENST00000679782.1:c.68T>C	ENSP00000505995.1:p.Leu23Pro
ENST00000679928.1:c.68T>C	ENSP00000506071.1:p.Leu23Pro
ENST00000680528.1:n.93T>C
ENST00000680999.1:c.68T>C	ENSP00000504984.1:p.Leu23Pro
ENST00000681282.1:c.68T>C	ENSP00000506339.1:p.Leu23Pro
ENST00000333213.10:c.68T>C	ENSP00000327487.6:p.Leu23Pro
ENST00000434205.7:c.-82-252T>C	ENSP00000406559.3:n.-82-252T>C
ENST00000580013.5:n.93T>C
ENST00000583173.5:c.56+141T>C	ENSP00000463619.1:n.56+141T>C
ENST00000583454.1:n.103T>C
NM_207346.2:c.68T>C	NP_997229.2:p.Leu23Pro
XM_005257229.2:c.68T>C	XP_005257286.1:p.Leu23Pro
XM_006721821.2:c.-236T>C	XP_006721884.1:n.-236T>C
XM_011524616.1:c.68T>C	XP_011522918.1:p.Leu23Pro
XM_011524617.1:c.68T>C	XP_011522919.1:p.Leu23Pro
XM_011524618.1:c.68T>C	XP_011522920.1:p.Leu23Pro
XR_243646.2:n.98T>C
XM_005257229.4:c.68T>C	XP_005257286.1:p.Leu23Pro
XR_243646.4:n.104T>C
NM_207346.3:c.68T>C MANE Select	NP_997229.2:p.Leu23Pro