Canonical Allele Identifier: CA10621869

Gene: LIFR

Linked Data

• ClinVar Variation Id: 353607
• ClinVar RCV Id: RCV000291427
• dbSNP Id: rs886060626
• MyVariant Identifiers: chr5:g.38481909A>T (hg19) ; chr5:g.38481807A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38481807A>T , CM000667.2:g.38481807A>T	GRCh38
NC_000005.9:g.38481909A>T , CM000667.1:g.38481909A>T	GRCh37
NC_000005.8:g.38517666A>T	NCBI36
NG_011817.1:g.118599T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000453190.7:c.3082T>A MANE Select	ENSP00000398368.2:p.Tyr1028Asn
ENST00000263409.8:c.3082T>A	ENSP00000263409.4:p.Tyr1028Asn
ENST00000453190.6:c.3082T>A	ENSP00000398368.2:p.Tyr1028Asn
NM_001127671.1:c.3082T>A	NP_001121143.1:p.Tyr1028Asn
NM_002310.5:c.3082T>A	NP_002301.1:p.Tyr1028Asn
XM_011514040.1:c.3082T>A	XP_011512342.1:p.Tyr1028Asn
XM_011514041.1:c.3082T>A	XP_011512343.1:p.Tyr1028Asn
XM_011514042.1:c.3082T>A	XP_011512344.1:p.Tyr1028Asn
NM_001364297.1:c.3082T>A	NP_001351226.1:p.Tyr1028Asn
NM_001364298.1:c.3049T>A	NP_001351227.1:p.Tyr1017Asn
XM_011514042.3:c.3082T>A	XP_011512344.1:p.Tyr1028Asn
XM_017009462.1:c.3136T>A	XP_016864951.1:p.Tyr1046Asn
XM_017009463.1:c.3082T>A	XP_016864952.1:p.Tyr1028Asn
NM_001127671.2:c.3082T>A MANE Select	NP_001121143.1:p.Tyr1028Asn
NM_002310.6:c.3082T>A	NP_002301.1:p.Tyr1028Asn
NM_001364297.2:c.3082T>A	NP_001351226.1:p.Tyr1028Asn
NM_001364298.2:c.3049T>A	NP_001351227.1:p.Tyr1017Asn