Canonical Allele Identifier: CA1540248688

Gene: LIFR

Linked Data

• dbSNP Id: rs1743982995

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38481557T>G , CM000667.2:g.38481557T>G	GRCh38
NC_000005.9:g.38481659T>G , CM000667.1:g.38481659T>G	GRCh37
NC_000005.8:g.38517416T>G	NCBI36
NG_011817.1:g.118849A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453190.7:c.*38A>C MANE Select	ENSP00000398368.2:n.*38A>C
ENST00000263409.8:c.*38A>C	ENSP00000263409.4:n.*38A>C
ENST00000453190.6:c.*38A>C	ENSP00000398368.2:n.*38A>C
NM_001127671.1:c.*38A>C	NP_001121143.1:n.*38A>C
NM_002310.5:c.*38A>C	NP_002301.1:n.*38A>C
XM_011514040.1:c.*38A>C	XP_011512342.1:n.*38A>C
XM_011514041.1:c.*38A>C	XP_011512343.1:n.*38A>C
XM_011514042.1:c.*38A>C	XP_011512344.1:n.*38A>C
NM_001364297.1:c.*38A>C	NP_001351226.1:n.*38A>C
NM_001364298.1:c.*38A>C	NP_001351227.1:n.*38A>C
XM_011514042.3:c.*38A>C	XP_011512344.1:n.*38A>C
XM_017009462.1:c.*38A>C	XP_016864951.1:n.*38A>C
XM_017009463.1:c.*38A>C	XP_016864952.1:n.*38A>C
NM_001127671.2:c.*38A>C MANE Select	NP_001121143.1:n.*38A>C
NM_002310.6:c.*38A>C	NP_002301.1:n.*38A>C
NM_001364297.2:c.*38A>C	NP_001351226.1:n.*38A>C
NM_001364298.2:c.*38A>C	NP_001351227.1:n.*38A>C