Canonical Allele Identifier: CA388221047

Gene: TNFSF11

Linked Data

• MyVariant Identifiers: chr13:g.43180704A>C (hg19) ; chr13:g.42606568A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.42606568A>C , CM000675.2:g.42606568A>C	GRCh38
NC_000013.10:g.43180704A>C , CM000675.1:g.43180704A>C	GRCh37
NC_000013.9:g.42078704A>C	NCBI36
NG_008990.1:g.48833A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000398795.7:c.604A>C MANE Select	ENSP00000381775.3:p.Ser202Arg
ENST00000239849.8:c.463A>C	ENSP00000239849.7:p.Ser155Arg
ENST00000358545.6:c.385A>C	ENSP00000351347.2:p.Ser129Arg
ENST00000398795.6:c.604A>C	ENSP00000381775.3:p.Ser202Arg
ENST00000405262.6:c.385A>C	ENSP00000384042.2:p.Ser129Arg
ENST00000544862.5:c.385A>C	ENSP00000444913.1:p.Ser129Arg
NM_003701.3:c.604A>C	NP_003692.1:p.Ser202Arg
NM_033012.3:c.385A>C	NP_143026.1:p.Ser129Arg
XM_011535280.1:c.385A>C	XP_011533582.1:p.Ser129Arg
XM_011535280.2:c.385A>C	XP_011533582.1:p.Ser129Arg
XM_017020802.1:c.442A>C	XP_016876291.1:p.Ser148Arg
XM_017020803.2:c.385A>C	XP_016876292.1:p.Ser129Arg
NM_003701.4:c.604A>C MANE Select	NP_003692.1:p.Ser202Arg
NM_033012.4:c.385A>C	NP_143026.1:p.Ser129Arg