Canonical Allele Identifier: CA8983938

Gene: TNFRSF11A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.62369171T>G , CM000680.2:g.62369171T>G	GRCh38
NC_000018.9:g.60036404T>G , CM000680.1:g.60036404T>G	GRCh37
NC_000018.8:g.58187384T>G	NCBI36
NG_008098.1:g.48857T>G , LRG_194:g.48857T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003839.4:c.1254T>G MANE Select	NP_003830.1:p.Ser418=
ENST00000586569.3:c.1254T>G MANE Select	ENSP00000465500.1:p.Ser418=
NM_001270949.1:c.783+2411T>G	NP_001257878.1:n.783+2411T>G
NM_001270949.2:c.783+2411T>G	NP_001257878.1:n.783+2411T>G
NM_001270950.1:c.730+7378T>G	NP_001257879.1:n.730+7378T>G
NM_001270950.2:c.730+7378T>G	NP_001257879.1:n.730+7378T>G
NM_001270951.1:c.616+9122T>G	NP_001257880.1:n.616+9122T>G
NM_001270951.2:c.616+9122T>G	NP_001257880.1:n.616+9122T>G
NM_001278268.1:c.1212T>G	NP_001265197.1:p.Ser404=
NM_001278268.2:c.1212T>G	NP_001265197.1:p.Ser404=
NM_003839.3:c.1254T>G	NP_003830.1:p.Ser418=
ENST00000269485.11:c.616+9122T>G	ENSP00000269485.7:n.616+9122T>G
ENST00000586569.2:c.1254T>G	ENSP00000465500.1:p.Ser418=
ENST00000616710.4:c.783+2411T>G	ENSP00000479567.1:n.783+2411T>G
ENST00000617039.4:c.730+7378T>G	ENSP00000482466.1:n.730+7378T>G
XM_011526244.1:c.1269T>G	XP_011524546.1:p.Ser423=
XM_011526244.2:c.1269T>G	XP_011524546.1:p.Ser423=
XM_011526245.1:c.1146T>G	XP_011524547.1:p.Ser382=
XM_011526245.2:c.1146T>G	XP_011524547.1:p.Ser382=
XM_017026064.1:c.1146T>G	XP_016881553.1:p.Ser382=
XM_017026065.1:c.1104T>G	XP_016881554.1:p.Ser368=
XM_017026066.1:c.1044T>G	XP_016881555.1:p.Ser348=
XR_935263.1:n.1284T>G