Canonical Allele Identifier: CA301715053

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62325385G>C , CM000680.2:g.62325385G>C	GRCh38
NC_000018.9:g.59992618G>C , CM000680.1:g.59992618G>C	GRCh37
NC_000018.8:g.58143598G>C	NCBI36
NG_008098.1:g.5071G>C , LRG_194:g.5071G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.33G>C MANE Select	NP_003830.1:p.Leu11=
ENST00000586569.3:c.33G>C MANE Select	ENSP00000465500.1:p.Leu11=
NM_001270949.1:c.33G>C	NP_001257878.1:p.Leu11=
NM_001270949.2:c.33G>C	NP_001257878.1:p.Leu11=
NM_001270950.1:c.33G>C	NP_001257879.1:p.Leu11=
NM_001270950.2:c.33G>C	NP_001257879.1:p.Leu11=
NM_001270951.1:c.33G>C	NP_001257880.1:p.Leu11=
NM_001270951.2:c.33G>C	NP_001257880.1:p.Leu11=
NM_001278268.1:c.33G>C	NP_001265197.1:p.Leu11=
NM_001278268.2:c.33G>C	NP_001265197.1:p.Leu11=
NM_003839.3:c.33G>C	NP_003830.1:p.Leu11=
ENST00000269485.11:c.33G>C	ENSP00000269485.7:p.Leu11=
ENST00000586569.2:c.33G>C	ENSP00000465500.1:p.Leu11=
ENST00000592013.1:n.60G>C
ENST00000616710.4:c.33G>C	ENSP00000479567.1:p.Leu11=
ENST00000617039.4:c.33G>C	ENSP00000482466.1:p.Leu11=
ENST00000639222.1:c.33G>C	ENSP00000492422.1:p.Leu11=
XM_011526244.1:c.33G>C	XP_011524546.1:p.Leu11=
XM_011526244.2:c.33G>C	XP_011524546.1:p.Leu11=
XM_011526245.1:c.-160G>C	XP_011524547.1:n.-160G>C
XM_011526245.2:c.-160G>C	XP_011524547.1:n.-160G>C
XR_935263.1:n.48G>C