Canonical Allele Identifier: CA1540244455

Gene: LIFR

Linked Data

• dbSNP Id: rs947910934

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38476510C>G , CM000667.2:g.38476510C>G	GRCh38
NC_000005.9:g.38476612C>G , CM000667.1:g.38476612C>G	GRCh37
NC_000005.8:g.38512369C>G	NCBI36
NG_011817.1:g.123896G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000453190.7:c.*5085G>C MANE Select	ENSP00000398368.2:n.*5085G>C
ENST00000263409.8:c.*5085G>C	ENSP00000263409.4:n.*5085G>C
NM_001127671.1:c.*5085G>C	NP_001121143.1:n.*5085G>C
NM_002310.5:c.*5085G>C	NP_002301.1:n.*5085G>C
XM_011514040.1:c.*5085G>C	XP_011512342.1:n.*5085G>C
XM_011514041.1:c.*5085G>C	XP_011512343.1:n.*5085G>C
XM_011514042.1:c.*5085G>C	XP_011512344.1:n.*5085G>C
NM_001364297.1:c.*5085G>C	NP_001351226.1:n.*5085G>C
NM_001364298.1:c.*5085G>C	NP_001351227.1:n.*5085G>C
XM_017009462.1:c.*5085G>C	XP_016864951.1:n.*5085G>C
NM_001127671.2:c.*5085G>C MANE Select	NP_001121143.1:n.*5085G>C
NM_002310.6:c.*5085G>C	NP_002301.1:n.*5085G>C
NM_001364297.2:c.*5085G>C	NP_001351226.1:n.*5085G>C
NM_001364298.2:c.*5085G>C	NP_001351227.1:n.*5085G>C