Canonical Allele Identifier: CA2308282849

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62354528C= , CM000680.2:g.62354528C=	GRCh38
NC_000018.9:g.60021761C= , CM000680.1:g.60021761C=	GRCh37
NC_000018.8:g.58172741C=	NCBI36
NG_008098.1:g.34214C= , LRG_194:g.34214C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.421C= MANE Select	NP_003830.1:p.His141=
ENST00000586569.3:c.421C= MANE Select	ENSP00000465500.1:p.His141=
NM_001270949.1:c.421C=	NP_001257878.1:p.His141=
NM_001270949.2:c.421C=	NP_001257878.1:p.His141=
NM_001270950.1:c.421C=	NP_001257879.1:p.His141=
NM_001270950.2:c.421C=	NP_001257879.1:p.His141=
NM_001270951.1:c.421C=	NP_001257880.1:p.His141=
NM_001270951.2:c.421C=	NP_001257880.1:p.His141=
NM_001278268.1:c.421C=	NP_001265197.1:p.His141=
NM_001278268.2:c.421C=	NP_001265197.1:p.His141=
NM_003839.3:c.421C=	NP_003830.1:p.His141=
ENST00000269485.11:c.421C=	ENSP00000269485.7:p.His141=
ENST00000586569.2:c.421C=	ENSP00000465500.1:p.His141=
ENST00000616710.4:c.421C=	ENSP00000479567.1:p.His141=
ENST00000617039.4:c.421C=	ENSP00000482466.1:p.His141=
ENST00000639222.1:c.421C=	ENSP00000492422.1:p.His141=
XM_011526244.1:c.421C=	XP_011524546.1:p.His141=
XM_011526244.2:c.421C=	XP_011524546.1:p.His141=
XM_011526245.1:c.303C=	XP_011524547.1:p.Ser101=
XM_011526245.2:c.303C=	XP_011524547.1:p.Ser101=
XM_017026064.1:c.303C=	XP_016881553.1:p.Ser101=
XM_017026065.1:c.256C=	XP_016881554.1:p.His86=
XM_017026066.1:c.201C=	XP_016881555.1:p.Ser67=
XR_935263.1:n.436C=