Canonical Allele Identifier: CA379859396

Gene: FAR1

Linked Data

• MyVariant Identifiers: chr11:g.13750222T>G (hg19) ; chr11:g.13728675T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728675T>G , CM000673.2:g.13728675T>G	GRCh38
NC_000011.9:g.13750222T>G , CM000673.1:g.13750222T>G	GRCh37
NC_000011.8:g.13706798T>G	NCBI36
NG_041826.1:g.65017T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*274T>G	ENSP00000515269.1:n.*274T>G
ENST00000354817.8:c.1449T>G MANE Select	ENSP00000346874.3:p.Ile483Met
ENST00000354817.7:c.1449T>G	ENSP00000346874.3:p.Ile483Met
ENST00000532502.1:c.321T>G	ENSP00000434624.1:p.Ile107Met
NM_032228.5:c.1449T>G	NP_115604.1:p.Ile483Met
XM_011520400.1:c.1458T>G	XP_011518702.1:p.Ile486Met
XM_011520401.1:c.1281T>G	XP_011518703.1:p.Ile427Met
XM_011520400.2:c.1458T>G	XP_011518702.1:p.Ile486Met
NM_032228.6:c.1449T>G MANE Select	NP_115604.1:p.Ile483Met