Canonical Allele Identifier: CA359539317
Gene: LIFR HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.38493858T>G (hg19) chr5:g.38493756T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.38493756T>G , CM000667.2:g.38493756T>G GRCh38
NC_000005.9:g.38493858T>G , CM000667.1:g.38493858T>G GRCh37
NC_000005.8:g.38529615T>G NCBI36
NG_011817.1:g.106650A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000453190.7:c.1915A>C MANE Select ENSP00000398368.2:p.Met639Leu
ENST00000263409.8:c.1915A>C ENSP00000263409.4:p.Met639Leu
ENST00000453190.6:c.1915A>C ENSP00000398368.2:p.Met639Leu
ENST00000503088.1:n.2078A>C
ENST00000506003.5:c.293A>C
NM_001127671.1:c.1915A>C NP_001121143.1:p.Met639Leu
NM_002310.5:c.1915A>C NP_002301.1:p.Met639Leu
XM_011514040.1:c.1915A>C XP_011512342.1:p.Met639Leu
XM_011514041.1:c.1915A>C XP_011512343.1:p.Met639Leu
XM_011514042.1:c.1915A>C XP_011512344.1:p.Met639Leu
NM_001364297.1:c.1915A>C NP_001351226.1:p.Met639Leu
NM_001364298.1:c.1915A>C NP_001351227.1:p.Met639Leu
XM_011514042.3:c.1915A>C XP_011512344.1:p.Met639Leu
XM_017009462.1:c.1969A>C XP_016864951.1:p.Met657Leu
XM_017009463.1:c.1915A>C XP_016864952.1:p.Met639Leu
NM_001127671.2:c.1915A>C MANE Select NP_001121143.1:p.Met639Leu
NM_002310.6:c.1915A>C NP_002301.1:p.Met639Leu
NM_001364297.2:c.1915A>C NP_001351226.1:p.Met639Leu
NM_001364298.2:c.1915A>C NP_001351227.1:p.Met639Leu
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