Canonical Allele Identifier: CA3243313
Gene: LIFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.38528873_38528878del , CM000667.2:g.38528873_38528878del GRCh38
NC_000005.9:g.38528975_38528980del , CM000667.1:g.38528975_38528980del GRCh37
NC_000005.8:g.38564732_38564737del NCBI36
NG_011817.1:g.71551_71556del

Transcript Alleles

HGVS Amino-acid Change
ENST00000453190.7:c.143-15_143-10del MANE Select ENSP00000398368.2:n.143-15_143-10del
ENST00000263409.8:c.143-15_143-10del ENSP00000263409.4:n.143-15_143-10del
ENST00000453190.6:c.143-15_143-10del ENSP00000398368.2:n.143-15_143-10del
ENST00000503088.1:n.306-15_306-10del
ENST00000506990.5:c.143-15_143-10del ENSP00000426685.1:n.143-15_143-10del
ENST00000511561.1:c.143-15_143-10del ENSP00000427310.1:n.143-15_143-10del
ENST00000512723.1:n.413-15_413-10del
NM_001127671.1:c.143-15_143-10del NP_001121143.1:n.143-15_143-10del
NM_002310.5:c.143-15_143-10del NP_002301.1:n.143-15_143-10del
XM_011514040.1:c.143-15_143-10del XP_011512342.1:n.143-15_143-10del
XM_011514041.1:c.143-15_143-10del XP_011512343.1:n.143-15_143-10del
XM_011514042.1:c.143-15_143-10del XP_011512344.1:n.143-15_143-10del
NM_001364297.1:c.143-15_143-10del NP_001351226.1:n.143-15_143-10del
NM_001364298.1:c.143-15_143-10del NP_001351227.1:n.143-15_143-10del
XM_011514042.3:c.143-15_143-10del XP_011512344.1:n.143-15_143-10del
XM_017009462.1:c.197-15_197-10del XP_016864951.1:n.197-15_197-10del
XM_017009463.1:c.143-15_143-10del XP_016864952.1:n.143-15_143-10del
NM_001127671.2:c.143-15_143-10del MANE Select NP_001121143.1:n.143-15_143-10del
NM_002310.6:c.143-15_143-10del NP_002301.1:n.143-15_143-10del
NM_001364297.2:c.143-15_143-10del NP_001351226.1:n.143-15_143-10del
NM_001364298.2:c.143-15_143-10del NP_001351227.1:n.143-15_143-10del