Canonical Allele Identifier: CA1540244440

Gene: LIFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38476479G= , CM000667.2:g.38476479G=	GRCh38
NC_000005.9:g.38476581G= , CM000667.1:g.38476581G=	GRCh37
NC_000005.8:g.38512338G=	NCBI36
NG_011817.1:g.123927C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000453190.7:c.*5116C= MANE Select	ENSP00000398368.2:n.*5116C=
ENST00000263409.8:c.*5116C=	ENSP00000263409.4:n.*5116C=
NM_001127671.1:c.*5116C=	NP_001121143.1:n.*5116C=
NM_002310.5:c.*5116C=	NP_002301.1:n.*5116C=
XM_011514040.1:c.*5116C=	XP_011512342.1:n.*5116C=
XM_011514041.1:c.*5116C=	XP_011512343.1:n.*5116C=
XM_011514042.1:c.*5116C=	XP_011512344.1:n.*5116C=
NM_001364297.1:c.*5116C=	NP_001351226.1:n.*5116C=
NM_001364298.1:c.*5116C=	NP_001351227.1:n.*5116C=
XM_017009462.1:c.*5116C=	XP_016864951.1:n.*5116C=
NM_001127671.2:c.*5116C= MANE Select	NP_001121143.1:n.*5116C=
NM_002310.6:c.*5116C=	NP_002301.1:n.*5116C=
NM_001364297.2:c.*5116C=	NP_001351226.1:n.*5116C=
NM_001364298.2:c.*5116C=	NP_001351227.1:n.*5116C=