Canonical Allele Identifier: CA1540254476

Gene: LIFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38485923A= , CM000667.2:g.38485923A=	GRCh38
NC_000005.9:g.38486025A= , CM000667.1:g.38486025A=	GRCh37
NC_000005.8:g.38521782A=	NCBI36
NG_011817.1:g.114483T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453190.7:c.2393T= MANE Select	ENSP00000398368.2:p.Ile798=
ENST00000263409.8:c.2393T=	ENSP00000263409.4:p.Ile798=
ENST00000453190.6:c.2393T=	ENSP00000398368.2:p.Ile798=
ENST00000508477.5:n.226T=
NM_001127671.1:c.2393T=	NP_001121143.1:p.Ile798=
NM_002310.5:c.2393T=	NP_002301.1:p.Ile798=
XM_011514040.1:c.2393T=	XP_011512342.1:p.Ile798=
XM_011514041.1:c.2393T=	XP_011512343.1:p.Ile798=
XM_011514042.1:c.2393T=	XP_011512344.1:p.Ile798=
NM_001364297.1:c.2393T=	NP_001351226.1:p.Ile798=
NM_001364298.1:c.2393T=	NP_001351227.1:p.Ile798=
XM_011514042.3:c.2393T=	XP_011512344.1:p.Ile798=
XM_017009462.1:c.2447T=	XP_016864951.1:p.Ile816=
XM_017009463.1:c.2393T=	XP_016864952.1:p.Ile798=
NM_001127671.2:c.2393T= MANE Select	NP_001121143.1:p.Ile798=
NM_002310.6:c.2393T=	NP_002301.1:p.Ile798=
NM_001364297.2:c.2393T=	NP_001351226.1:p.Ile798=
NM_001364298.2:c.2393T=	NP_001351227.1:p.Ile798=