Canonical Allele Identifier: CA379859402

Gene: FAR1

Linked Data

• dbSNP Id: rs1298121454
• gnomAD v2: 11-13750224-C-T
• gnomAD v4: 11-13728677-C-T
• MyVariant Identifiers: chr11:g.13750224C>T (hg19) ; chr11:g.13728677C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728677C>T , CM000673.2:g.13728677C>T	GRCh38
NC_000011.9:g.13750224C>T , CM000673.1:g.13750224C>T	GRCh37
NC_000011.8:g.13706800C>T	NCBI36
NG_041826.1:g.65019C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*276C>T	ENSP00000515269.1:n.*276C>T
ENST00000354817.8:c.1451C>T MANE Select	ENSP00000346874.3:p.Ala484Val
ENST00000354817.7:c.1451C>T	ENSP00000346874.3:p.Ala484Val
ENST00000532502.1:c.323C>T	ENSP00000434624.1:p.Ala108Val
NM_032228.5:c.1451C>T	NP_115604.1:p.Ala484Val
XM_011520400.1:c.1460C>T	XP_011518702.1:p.Ala487Val
XM_011520401.1:c.1283C>T	XP_011518703.1:p.Ala428Val
XM_011520400.2:c.1460C>T	XP_011518702.1:p.Ala487Val
NM_032228.6:c.1451C>T MANE Select	NP_115604.1:p.Ala484Val