Canonical Allele Identifier: CA597905990

Gene: FAR1

Linked Data

• dbSNP Id: rs1388770179
• gnomAD v2: 11-13750129-G-A
• gnomAD v3: 11-13728582-G-A
• gnomAD v4: 11-13728582-G-A
• MyVariant Identifiers: chr11:g.13750129G>A (hg19) ; chr11:g.13728582G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.13728582G>A , CM000673.2:g.13728582G>A	GRCh38
NC_000011.9:g.13750129G>A , CM000673.1:g.13750129G>A	GRCh37
NC_000011.8:g.13706705G>A	NCBI36
NG_041826.1:g.64924G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703358.1:c.*211-30G>A	ENSP00000515269.1:n.*211-30G>A
ENST00000354817.8:c.1386-30G>A MANE Select	ENSP00000346874.3:n.1386-30G>A
ENST00000354817.7:c.1386-30G>A	ENSP00000346874.3:n.1386-30G>A
ENST00000532502.1:c.258-30G>A	ENSP00000434624.1:n.258-30G>A
NM_032228.5:c.1386-30G>A	NP_115604.1:n.1386-30G>A
XM_011520400.1:c.1395-30G>A	XP_011518702.1:n.1395-30G>A
XM_011520401.1:c.1218-30G>A	XP_011518703.1:n.1218-30G>A
XM_011520400.2:c.1395-30G>A	XP_011518702.1:n.1395-30G>A
NM_032228.6:c.1386-30G>A MANE Select	NP_115604.1:n.1386-30G>A