Canonical Allele Identifier: CA1679165

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61839613T>C , CM000664.2:g.61839613T>C	GRCh38
NC_000002.11:g.62066748T>C , CM000664.1:g.62066748T>C	GRCh37
NC_000002.10:g.61920252T>C	NCBI36
NG_028125.1:g.19531A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1391A>G MANE Select	NP_001188472.1:p.His464Arg
ENST00000404929.6:c.1391A>G MANE Select	ENSP00000385158.1:p.His464Arg
NM_001201543.1:c.1391A>G	NP_001188472.1:p.His464Arg
NM_032180.2:c.1391A>G	NP_115556.2:p.His464Arg
NM_032180.3:c.1391A>G	NP_115556.2:p.His464Arg
NR_037710.1:n.1437A>G
NR_037710.2:n.1354A>G
ENST00000307507.3:c.*1401A>G	ENSP00000303170.3:n.*1401A>G
ENST00000404929.5:c.1391A>G	ENSP00000385158.1:p.His464Arg
ENST00000405894.3:c.1391A>G	ENSP00000385893.3:p.His464Arg
ENST00000418113.5:c.1378A>G
ENST00000456262.5:c.*906A>G	ENSP00000396105.1:n.*906A>G
XM_017005072.1:c.1064A>G	XP_016860561.1:p.His355Arg
XM_017005073.1:c.821A>G	XP_016860562.1:p.His274Arg
XM_017005074.1:c.821A>G	XP_016860563.1:p.His274Arg
XR_001738972.2:n.1392A>G
XR_001738973.2:n.1392A>G
XR_001738974.2:n.1392A>G
XR_001738975.2:n.1392A>G
XR_001738976.1:n.1420A>G
XR_001738977.1:n.1420A>G
XR_939724.1:n.2752A>G