Canonical Allele Identifier: CA1679142

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61839520C>T , CM000664.2:g.61839520C>T	GRCh38
NC_000002.11:g.62066655C>T , CM000664.1:g.62066655C>T	GRCh37
NC_000002.10:g.61920159C>T	NCBI36
NG_028125.1:g.19624G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1484G>A MANE Select	NP_001188472.1:p.Arg495His
ENST00000404929.6:c.1484G>A MANE Select	ENSP00000385158.1:p.Arg495His
NM_001201543.1:c.1484G>A	NP_001188472.1:p.Arg495His
NM_032180.2:c.1484G>A	NP_115556.2:p.Arg495His
NM_032180.3:c.1484G>A	NP_115556.2:p.Arg495His
NR_037710.1:n.1530G>A
NR_037710.2:n.1447G>A
ENST00000307507.3:c.*1494G>A	ENSP00000303170.3:n.*1494G>A
ENST00000404929.5:c.1484G>A	ENSP00000385158.1:p.Arg495His
ENST00000405894.3:c.1484G>A	ENSP00000385893.3:p.Arg495His
ENST00000418113.5:c.1471G>A
ENST00000456262.5:c.*999G>A	ENSP00000396105.1:n.*999G>A
ENST00000496369.1:n.5G>A
XM_017005072.1:c.1157G>A	XP_016860561.1:p.Arg386His
XM_017005073.1:c.914G>A	XP_016860562.1:p.Arg305His
XM_017005074.1:c.914G>A	XP_016860563.1:p.Arg305His
XR_001738972.2:n.1485G>A
XR_001738973.2:n.1485G>A
XR_001738974.2:n.1485G>A
XR_001738975.2:n.1485G>A
XR_001738976.1:n.1513G>A
XR_001738977.1:n.1513G>A
XR_939724.1:n.2845G>A