Canonical Allele Identifier: CA379859381

Gene: FAR1

Linked Data

• MyVariant Identifiers: chr11:g.13750216T>G (hg19) ; chr11:g.13728669T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728669T>G , CM000673.2:g.13728669T>G	GRCh38
NC_000011.9:g.13750216T>G , CM000673.1:g.13750216T>G	GRCh37
NC_000011.8:g.13706792T>G	NCBI36
NG_041826.1:g.65011T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*268T>G	ENSP00000515269.1:n.*268T>G
ENST00000354817.8:c.1443T>G MANE Select	ENSP00000346874.3:p.Ile481Met
ENST00000354817.7:c.1443T>G	ENSP00000346874.3:p.Ile481Met
ENST00000532502.1:c.315T>G	ENSP00000434624.1:p.Ile105Met
NM_032228.5:c.1443T>G	NP_115604.1:p.Ile481Met
XM_011520400.1:c.1452T>G	XP_011518702.1:p.Ile484Met
XM_011520401.1:c.1275T>G	XP_011518703.1:p.Ile425Met
XM_011520400.2:c.1452T>G	XP_011518702.1:p.Ile484Met
NM_032228.6:c.1443T>G MANE Select	NP_115604.1:p.Ile481Met