Canonical Allele Identifier: CA346985844

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61838538C>T , CM000664.2:g.61838538C>T	GRCh38
NC_000002.11:g.62065673C>T , CM000664.1:g.62065673C>T	GRCh37
NC_000002.10:g.61919177C>T	NCBI36
NG_028125.1:g.20606G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1751G>A MANE Select	NP_001188472.1:p.Arg584Lys
ENST00000404929.6:c.1751G>A MANE Select	ENSP00000385158.1:p.Arg584Lys
NM_001201543.1:c.1751G>A	NP_001188472.1:p.Arg584Lys
NM_032180.2:c.1583+883G>A	NP_115556.2:n.1583+883G>A
NM_032180.3:c.1583+883G>A	NP_115556.2:n.1583+883G>A
NR_037710.1:n.1629+883G>A
NR_037710.2:n.1546+883G>A
ENST00000307507.3:c.*1593+883G>A	ENSP00000303170.3:n.*1593+883G>A
ENST00000404929.5:c.1751G>A	ENSP00000385158.1:p.Arg584Lys
ENST00000405894.3:c.1583+883G>A	ENSP00000385893.3:n.1583+883G>A
ENST00000418113.5:c.1738G>A
ENST00000456262.5:c.*1098+883G>A	ENSP00000396105.1:n.*1098+883G>A
ENST00000496369.1:n.104+883G>A
XM_017005072.1:c.1256+883G>A	XP_016860561.1:n.1256+883G>A
XM_017005073.1:c.1181G>A	XP_016860562.1:p.Arg394Lys
XM_017005074.1:c.1013+883G>A	XP_016860563.1:n.1013+883G>A
XR_001738972.2:n.1752G>A
XR_001738973.2:n.1584+883G>A
XR_001738974.2:n.1752G>A
XR_001738975.2:n.1752G>A
XR_001738976.1:n.1780G>A
XR_001738977.1:n.1612+883G>A
XR_939724.1:n.3112G>A