Canonical Allele Identifier: CA402613717

Gene: TNFRSF11A

Linked Data

• MyVariant Identifiers: chr18:g.60027244T>C (hg19) ; chr18:g.62360011T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62360011T>C , CM000680.2:g.62360011T>C	GRCh38
NC_000018.9:g.60027244T>C , CM000680.1:g.60027244T>C	GRCh37
NC_000018.8:g.58178224T>C	NCBI36
NG_008098.1:g.39697T>C , LRG_194:g.39697T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586569.3:c.578T>C MANE Select	ENSP00000465500.1:p.Val193Ala
ENST00000639222.1:c.578T>C	ENSP00000492422.1:p.Val193Ala
ENST00000269485.11:c.578T>C	ENSP00000269485.7:p.Val193Ala
ENST00000586569.2:c.578T>C	ENSP00000465500.1:p.Val193Ala
ENST00000587697.1:n.496T>C
ENST00000616710.4:c.578T>C	ENSP00000479567.1:p.Val193Ala
ENST00000617039.4:c.578T>C	ENSP00000482466.1:p.Val193Ala
NM_001270949.1:c.578T>C	NP_001257878.1:p.Val193Ala
NM_001270950.1:c.578T>C	NP_001257879.1:p.Val193Ala
NM_001270951.1:c.578T>C	NP_001257880.1:p.Val193Ala
NM_001278268.1:c.536T>C	NP_001265197.1:p.Val179Ala
NM_003839.3:c.578T>C	NP_003830.1:p.Val193Ala
XM_011526244.1:c.593T>C	XP_011524546.1:p.Val198Ala
XM_011526245.1:c.470T>C	XP_011524547.1:p.Val157Ala
XR_935263.1:n.608T>C
XM_011526244.2:c.593T>C	XP_011524546.1:p.Val198Ala
XM_011526245.2:c.470T>C	XP_011524547.1:p.Val157Ala
XM_017026064.1:c.470T>C	XP_016881553.1:p.Val157Ala
XM_017026065.1:c.428T>C	XP_016881554.1:p.Val143Ala
XM_017026066.1:c.368T>C	XP_016881555.1:p.Val123Ala
NM_003839.4:c.578T>C MANE Select	NP_003830.1:p.Val193Ala
NM_001270951.2:c.578T>C	NP_001257880.1:p.Val193Ala
NM_001278268.2:c.536T>C	NP_001265197.1:p.Val179Ala
NM_001270949.2:c.578T>C	NP_001257878.1:p.Val193Ala
NM_001270950.2:c.578T>C	NP_001257879.1:p.Val193Ala