Canonical Allele Identifier: CA401029156

Gene: TSEN54

Linked Data

• MyVariant Identifiers: chr17:g.73517992G>C (hg19) ; chr17:g.75521911G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75521911G>C , CM000679.2:g.75521911G>C	GRCh38
NC_000017.10:g.73517992G>C , CM000679.1:g.73517992G>C	GRCh37
NC_000017.9:g.71029587G>C	NCBI36
NG_013041.1:g.10384G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000333213.11:c.830G>C MANE Select	ENSP00000327487.6:p.Cys277Ser
ENST00000434205.8:c.527G>C	ENSP00000406559.4:p.Cys176Ser
ENST00000545228.3:c.830G>C	ENSP00000438169.3:p.Cys277Ser
ENST00000579449.2:n.629G>C
ENST00000580013.6:n.1033G>C
ENST00000679370.1:n.1411G>C
ENST00000679429.1:c.*288G>C	ENSP00000505403.1:n.*288G>C
ENST00000679443.1:n.899G>C
ENST00000679782.1:c.830G>C	ENSP00000505995.1:p.Cys277Ser
ENST00000679919.1:n.899G>C
ENST00000679928.1:c.*441G>C	ENSP00000506071.1:n.*441G>C
ENST00000680528.1:n.855G>C
ENST00000680999.1:c.830G>C	ENSP00000504984.1:p.Cys277Ser
ENST00000681282.1:c.*76G>C	ENSP00000506339.1:n.*76G>C
ENST00000333213.10:c.830G>C	ENSP00000327487.6:p.Cys277Ser
ENST00000578415.1:c.790G>C
ENST00000583173.5:c.459-96G>C	ENSP00000463619.1:n.459-96G>C
NM_207346.2:c.830G>C	NP_997229.2:p.Cys277Ser
XM_005257229.2:c.830G>C	XP_005257286.1:p.Cys277Ser
XM_006721821.2:c.527G>C	XP_006721884.1:p.Cys176Ser
XM_011524616.1:c.830G>C	XP_011522918.1:p.Cys277Ser
XM_011524617.1:c.830G>C	XP_011522919.1:p.Cys277Ser
XM_011524618.1:c.830G>C	XP_011522920.1:p.Cys277Ser
XR_243646.2:n.860G>C
XM_005257229.4:c.830G>C	XP_005257286.1:p.Cys277Ser
XR_243646.4:n.866G>C
NM_207346.3:c.830G>C MANE Select	NP_997229.2:p.Cys277Ser