Canonical Allele Identifier: CA359533342

Gene: LIFR

Linked Data

• MyVariant Identifiers: chr5:g.38481827A>G (hg19) ; chr5:g.38481725A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.38481725A>G , CM000667.2:g.38481725A>G	GRCh38
NC_000005.9:g.38481827A>G , CM000667.1:g.38481827A>G	GRCh37
NC_000005.8:g.38517584A>G	NCBI36
NG_011817.1:g.118681T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000453190.7:c.3164T>C MANE Select	ENSP00000398368.2:p.Val1055Ala
ENST00000263409.8:c.3164T>C	ENSP00000263409.4:p.Val1055Ala
ENST00000453190.6:c.3164T>C	ENSP00000398368.2:p.Val1055Ala
NM_001127671.1:c.3164T>C	NP_001121143.1:p.Val1055Ala
NM_002310.5:c.3164T>C	NP_002301.1:p.Val1055Ala
XM_011514040.1:c.3164T>C	XP_011512342.1:p.Val1055Ala
XM_011514041.1:c.3164T>C	XP_011512343.1:p.Val1055Ala
XM_011514042.1:c.3164T>C	XP_011512344.1:p.Val1055Ala
NM_001364297.1:c.3164T>C	NP_001351226.1:p.Val1055Ala
NM_001364298.1:c.3131T>C	NP_001351227.1:p.Val1044Ala
XM_011514042.3:c.3164T>C	XP_011512344.1:p.Val1055Ala
XM_017009462.1:c.3218T>C	XP_016864951.1:p.Val1073Ala
XM_017009463.1:c.3164T>C	XP_016864952.1:p.Val1055Ala
NM_001127671.2:c.3164T>C MANE Select	NP_001121143.1:p.Val1055Ala
NM_002310.6:c.3164T>C	NP_002301.1:p.Val1055Ala
NM_001364297.2:c.3164T>C	NP_001351226.1:p.Val1055Ala
NM_001364298.2:c.3131T>C	NP_001351227.1:p.Val1044Ala