Canonical Allele Identifier: CA1678977

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61827103C>T , CM000664.2:g.61827103C>T	GRCh38
NC_000002.11:g.62054238C>T , CM000664.1:g.62054238C>T	GRCh37
NC_000002.10:g.61907742C>T	NCBI36
NG_028125.1:g.32041G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.2006+1G>A MANE Select	NP_001188472.1:n.2006+1G>A
ENST00000404929.6:c.2006+1G>A MANE Select	ENSP00000385158.1:n.2006+1G>A
NM_001201543.1:c.2006+1G>A	NP_001188472.1:n.2006+1G>A
NM_032180.2:c.1838+1G>A	NP_115556.2:n.1838+1G>A
NM_032180.3:c.1838+1G>A	NP_115556.2:n.1838+1G>A
NR_037710.1:n.1884+1G>A
NR_037710.2:n.1801+1G>A
ENST00000404929.5:c.2006+1G>A	ENSP00000385158.1:n.2006+1G>A
ENST00000405894.3:c.1838+1G>A	ENSP00000385893.3:n.1838+1G>A
ENST00000418113.5:c.2283+1G>A
ENST00000456262.5:c.*1353+1G>A	ENSP00000396105.1:n.*1353+1G>A
XM_017005072.1:c.1511+1G>A	XP_016860561.1:n.1511+1G>A
XM_017005073.1:c.1436+1G>A	XP_016860562.1:n.1436+1G>A
XM_017005074.1:c.1268+1G>A	XP_016860563.1:n.1268+1G>A
XR_001738972.2:n.2007+1G>A
XR_001738973.2:n.1839+1G>A
XR_001738974.2:n.2007+1G>A
XR_001738976.1:n.2035+1G>A
XR_001738977.1:n.1867+1G>A
XR_939724.1:n.3367+1G>A