Canonical Allele Identifier: CA559046682

Gene: LIFR

Linked Data

• dbSNP Id: rs1476318857
• gnomAD v2: 5-38476604-C-T
• gnomAD v3: 5-38476502-C-T
• gnomAD v4: 5-38476502-C-T
• MyVariant Identifiers: chr5:g.38476604C>T (hg19) ; chr5:g.38476502C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38476502C>T , CM000667.2:g.38476502C>T	GRCh38
NC_000005.9:g.38476604C>T , CM000667.1:g.38476604C>T	GRCh37
NC_000005.8:g.38512361C>T	NCBI36
NG_011817.1:g.123904G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453190.7:c.*5093G>A MANE Select	ENSP00000398368.2:n.*5093G>A
ENST00000263409.8:c.*5093G>A	ENSP00000263409.4:n.*5093G>A
NM_001127671.1:c.*5093G>A	NP_001121143.1:n.*5093G>A
NM_002310.5:c.*5093G>A	NP_002301.1:n.*5093G>A
XM_011514040.1:c.*5093G>A	XP_011512342.1:n.*5093G>A
XM_011514041.1:c.*5093G>A	XP_011512343.1:n.*5093G>A
XM_011514042.1:c.*5093G>A	XP_011512344.1:n.*5093G>A
NM_001364297.1:c.*5093G>A	NP_001351226.1:n.*5093G>A
NM_001364298.1:c.*5093G>A	NP_001351227.1:n.*5093G>A
XM_017009462.1:c.*5093G>A	XP_016864951.1:n.*5093G>A
NM_001127671.2:c.*5093G>A MANE Select	NP_001121143.1:n.*5093G>A
NM_002310.6:c.*5093G>A	NP_002301.1:n.*5093G>A
NM_001364297.2:c.*5093G>A	NP_001351226.1:n.*5093G>A
NM_001364298.2:c.*5093G>A	NP_001351227.1:n.*5093G>A