Canonical Allele Identifier: CA1540249148

Gene: LIFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38481815G= , CM000667.2:g.38481815G=	GRCh38
NC_000005.9:g.38481917G= , CM000667.1:g.38481917G=	GRCh37
NC_000005.8:g.38517674G=	NCBI36
NG_011817.1:g.118591C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453190.7:c.3074C= MANE Select	ENSP00000398368.2:p.Thr1025=
ENST00000263409.8:c.3074C=	ENSP00000263409.4:p.Thr1025=
ENST00000453190.6:c.3074C=	ENSP00000398368.2:p.Thr1025=
NM_001127671.1:c.3074C=	NP_001121143.1:p.Thr1025=
NM_002310.5:c.3074C=	NP_002301.1:p.Thr1025=
XM_011514040.1:c.3074C=	XP_011512342.1:p.Thr1025=
XM_011514041.1:c.3074C=	XP_011512343.1:p.Thr1025=
XM_011514042.1:c.3074C=	XP_011512344.1:p.Thr1025=
NM_001364297.1:c.3074C=	NP_001351226.1:p.Thr1025=
NM_001364298.1:c.3041C=	NP_001351227.1:p.Thr1014=
XM_011514042.3:c.3074C=	XP_011512344.1:p.Thr1025=
XM_017009462.1:c.3128C=	XP_016864951.1:p.Thr1043=
XM_017009463.1:c.3074C=	XP_016864952.1:p.Thr1025=
NM_001127671.2:c.3074C= MANE Select	NP_001121143.1:p.Thr1025=
NM_002310.6:c.3074C=	NP_002301.1:p.Thr1025=
NM_001364297.2:c.3074C=	NP_001351226.1:p.Thr1025=
NM_001364298.2:c.3041C=	NP_001351227.1:p.Thr1014=