Canonical Allele Identifier: CA1540245372

Gene: LIFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38496336A= , CM000667.2:g.38496336A=	GRCh38
NC_000005.9:g.38496438A= , CM000667.1:g.38496438A=	GRCh37
NC_000005.8:g.38532195A=	NCBI36
NG_011817.1:g.104070T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453190.7:c.1885+46T= MANE Select	ENSP00000398368.2:n.1885+46T=
ENST00000263409.8:c.1885+46T=	ENSP00000263409.4:n.1885+46T=
ENST00000453190.6:c.1885+46T=	ENSP00000398368.2:n.1885+46T=
ENST00000503088.1:n.2048+46T=
ENST00000506003.5:c.263+46T=
NM_001127671.1:c.1885+46T=	NP_001121143.1:n.1885+46T=
NM_002310.5:c.1885+46T=	NP_002301.1:n.1885+46T=
XM_011514040.1:c.1885+46T=	XP_011512342.1:n.1885+46T=
XM_011514041.1:c.1885+46T=	XP_011512343.1:n.1885+46T=
XM_011514042.1:c.1885+46T=	XP_011512344.1:n.1885+46T=
NM_001364297.1:c.1885+46T=	NP_001351226.1:n.1885+46T=
NM_001364298.1:c.1885+46T=	NP_001351227.1:n.1885+46T=
XM_011514042.3:c.1885+46T=	XP_011512344.1:n.1885+46T=
XM_017009462.1:c.1939+46T=	XP_016864951.1:n.1939+46T=
XM_017009463.1:c.1885+46T=	XP_016864952.1:n.1885+46T=
NM_001127671.2:c.1885+46T= MANE Select	NP_001121143.1:n.1885+46T=
NM_002310.6:c.1885+46T=	NP_002301.1:n.1885+46T=
NM_001364297.2:c.1885+46T=	NP_001351226.1:n.1885+46T=
NM_001364298.2:c.1885+46T=	NP_001351227.1:n.1885+46T=