Canonical Allele Identifier: CA384346490

Gene: FAR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.29311888A>T , CM000674.2:g.29311888A>T	GRCh38
NC_000012.11:g.29464821A>T , CM000674.1:g.29464821A>T	GRCh37
NC_000012.10:g.29356088A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001271783.2:c.893A>T MANE Select	NP_001258712.1:p.Lys298Met
ENST00000536681.8:c.893A>T MANE Select	ENSP00000443291.2:p.Lys298Met
NM_001271783.1:c.893A>T	NP_001258712.1:p.Lys298Met
NM_001271784.1:c.602A>T	NP_001258713.1:p.Lys201Met
NM_001271784.2:c.602A>T	NP_001258713.1:p.Lys201Met
NM_018099.4:c.893A>T	NP_060569.3:p.Lys298Met
NM_018099.5:c.893A>T	NP_060569.3:p.Lys298Met
NR_103860.1:n.142-1985T>A
ENST00000182377.8:c.893A>T	ENSP00000182377.4:p.Lys298Met
ENST00000536681.7:c.893A>T	ENSP00000443291.2:p.Lys298Met
ENST00000547116.5:c.602A>T	ENSP00000449349.1:p.Lys201Met
ENST00000547759.2:c.893A>T	ENSP00000447467.2:p.Lys298Met
ENST00000551193.2:c.257A>T	ENSP00000449187.2:p.Lys86Met
ENST00000551451.6:c.893A>T	ENSP00000450117.2:p.Lys298Met
ENST00000685369.1:n.1204A>T
ENST00000686305.1:c.*324A>T	ENSP00000509385.1:n.*324A>T
ENST00000686316.1:n.3098A>T
ENST00000686419.1:c.893A>T	ENSP00000509644.1:p.Lys298Met
ENST00000686974.1:n.1323A>T
ENST00000689380.1:n.3775A>T
ENST00000689798.1:n.461A>T
ENST00000690002.1:n.3609A>T
ENST00000690162.1:c.602A>T	ENSP00000510233.1:p.Lys201Met
ENST00000691273.1:c.893A>T	ENSP00000508629.1:p.Lys298Met
ENST00000691325.1:n.1946A>T
ENST00000692223.1:c.893A>T	ENSP00000508868.1:p.Lys298Met
ENST00000693163.1:c.*510A>T	ENSP00000508704.1:n.*510A>T
XM_011520747.1:c.953A>T	XP_011519049.1:p.Lys318Met
XM_011520747.2:c.953A>T	XP_011519049.1:p.Lys318Met
XM_011520748.1:c.953A>T	XP_011519050.1:p.Lys318Met
XM_011520748.3:c.953A>T	XP_011519050.1:p.Lys318Met
XM_017019624.2:c.893A>T	XP_016875113.1:p.Lys298Met
XM_017019625.2:c.257A>T	XP_016875114.1:p.Lys86Met