Canonical Allele Identifier: CA402612986

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62358263A>T , CM000680.2:g.62358263A>T	GRCh38
NC_000018.9:g.60025496A>T , CM000680.1:g.60025496A>T	GRCh37
NC_000018.8:g.58176476A>T	NCBI36
NG_008098.1:g.37949A>T , LRG_194:g.37949A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.443A>T MANE Select	NP_003830.1:p.Asp148Val
ENST00000586569.3:c.443A>T MANE Select	ENSP00000465500.1:p.Asp148Val
NM_001270949.1:c.443A>T	NP_001257878.1:p.Asp148Val
NM_001270949.2:c.443A>T	NP_001257878.1:p.Asp148Val
NM_001270950.1:c.443A>T	NP_001257879.1:p.Asp148Val
NM_001270950.2:c.443A>T	NP_001257879.1:p.Asp148Val
NM_001270951.1:c.443A>T	NP_001257880.1:p.Asp148Val
NM_001270951.2:c.443A>T	NP_001257880.1:p.Asp148Val
NM_001278268.1:c.428-27A>T	NP_001265197.1:n.428-27A>T
NM_001278268.2:c.428-27A>T	NP_001265197.1:n.428-27A>T
NM_003839.3:c.443A>T	NP_003830.1:p.Asp148Val
ENST00000269485.11:c.443A>T	ENSP00000269485.7:p.Asp148Val
ENST00000586569.2:c.443A>T	ENSP00000465500.1:p.Asp148Val
ENST00000587697.1:n.361A>T
ENST00000616710.4:c.443A>T	ENSP00000479567.1:p.Asp148Val
ENST00000617039.4:c.443A>T	ENSP00000482466.1:p.Asp148Val
ENST00000639222.1:c.443A>T	ENSP00000492422.1:p.Asp148Val
XM_011526244.1:c.458A>T	XP_011524546.1:p.Asp153Val
XM_011526244.2:c.458A>T	XP_011524546.1:p.Asp153Val
XM_011526245.1:c.335A>T	XP_011524547.1:p.Asp112Val
XM_011526245.2:c.335A>T	XP_011524547.1:p.Asp112Val
XM_017026064.1:c.335A>T	XP_016881553.1:p.Asp112Val
XM_017026065.1:c.293A>T	XP_016881554.1:p.Asp98Val
XM_017026066.1:c.233A>T	XP_016881555.1:p.Asp78Val
XR_935263.1:n.473A>T