Canonical Allele Identifier: CA402613484

Gene: TNFRSF11A

Linked Data

• MyVariant Identifiers: chr18:g.60025576T>C (hg19) ; chr18:g.62358343T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62358343T>C , CM000680.2:g.62358343T>C	GRCh38
NC_000018.9:g.60025576T>C , CM000680.1:g.60025576T>C	GRCh37
NC_000018.8:g.58176556T>C	NCBI36
NG_008098.1:g.38029T>C , LRG_194:g.38029T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000586569.3:c.521+2T>C MANE Select	ENSP00000465500.1:n.521+2T>C
ENST00000639222.1:c.521+2T>C	ENSP00000492422.1:n.521+2T>C
ENST00000269485.11:c.521+2T>C	ENSP00000269485.7:n.521+2T>C
ENST00000586569.2:c.521+2T>C	ENSP00000465500.1:n.521+2T>C
ENST00000587697.1:n.439+2T>C
ENST00000616710.4:c.521+2T>C	ENSP00000479567.1:n.521+2T>C
ENST00000617039.4:c.521+2T>C	ENSP00000482466.1:n.521+2T>C
NM_001270949.1:c.521+2T>C	NP_001257878.1:n.521+2T>C
NM_001270950.1:c.521+2T>C	NP_001257879.1:n.521+2T>C
NM_001270951.1:c.521+2T>C	NP_001257880.1:n.521+2T>C
NM_001278268.1:c.479+2T>C	NP_001265197.1:n.479+2T>C
NM_003839.3:c.521+2T>C	NP_003830.1:n.521+2T>C
XM_011526244.1:c.536+2T>C	XP_011524546.1:n.536+2T>C
XM_011526245.1:c.413+2T>C	XP_011524547.1:n.413+2T>C
XR_935263.1:n.551+2T>C
XM_011526244.2:c.536+2T>C	XP_011524546.1:n.536+2T>C
XM_011526245.2:c.413+2T>C	XP_011524547.1:n.413+2T>C
XM_017026064.1:c.413+2T>C	XP_016881553.1:n.413+2T>C
XM_017026065.1:c.371+2T>C	XP_016881554.1:n.371+2T>C
XM_017026066.1:c.311+2T>C	XP_016881555.1:n.311+2T>C
NM_003839.4:c.521+2T>C MANE Select	NP_003830.1:n.521+2T>C
NM_001270951.2:c.521+2T>C	NP_001257880.1:n.521+2T>C
NM_001278268.2:c.479+2T>C	NP_001265197.1:n.479+2T>C
NM_001270949.2:c.521+2T>C	NP_001257878.1:n.521+2T>C
NM_001270950.2:c.521+2T>C	NP_001257879.1:n.521+2T>C