Canonical Allele Identifier: CA775078653

Gene: TSEN54

Linked Data

• dbSNP Id: rs1405496897
• MyVariant Identifiers: chr17:g.73520624T>C (hg19) ; chr17:g.75524543T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.75524543T>C , CM000679.2:g.75524543T>C	GRCh38
NC_000017.10:g.73520624T>C , CM000679.1:g.73520624T>C	GRCh37
NC_000017.9:g.71032219T>C	NCBI36
NG_013041.1:g.13016T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333213.11:c.*131T>C MANE Select	ENSP00000327487.6:n.*131T>C
ENST00000434205.8:c.*131T>C	ENSP00000406559.4:n.*131T>C
ENST00000545228.3:c.*211T>C	ENSP00000438169.3:n.*211T>C
ENST00000577197.2:n.910T>C
ENST00000579449.2:n.2452T>C
ENST00000580013.6:n.2856T>C
ENST00000679370.1:n.3234T>C
ENST00000679429.1:c.*1170T>C	ENSP00000505403.1:n.*1170T>C
ENST00000679443.1:n.1781T>C
ENST00000679782.1:c.*411T>C	ENSP00000505995.1:n.*411T>C
ENST00000679919.1:n.1983T>C
ENST00000679928.1:c.*2264T>C	ENSP00000506071.1:n.*2264T>C
ENST00000680999.1:c.*131T>C	ENSP00000504984.1:n.*131T>C
ENST00000681282.1:c.*1899T>C	ENSP00000506339.1:n.*1899T>C
ENST00000333213.10:c.*131T>C	ENSP00000327487.6:n.*131T>C
ENST00000545228.2:c.989T>C
ENST00000577197.1:n.460T>C
NM_207346.2:c.*131T>C	NP_997229.2:n.*131T>C
XM_005257229.2:c.*211T>C	XP_005257286.1:n.*211T>C
XM_006721821.2:c.*211T>C	XP_006721884.1:n.*211T>C
XM_011524616.1:c.*211T>C	XP_011522918.1:n.*211T>C
XM_011524618.1:c.*131T>C	XP_011522920.1:n.*131T>C
XR_243646.2:n.1944T>C
XM_005257229.4:c.*211T>C	XP_005257286.1:n.*211T>C
XR_243646.4:n.1950T>C
NM_207346.3:c.*131T>C MANE Select	NP_997229.2:n.*131T>C