Canonical Allele Identifier: CA346985016

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61827260T>A , CM000664.2:g.61827260T>A	GRCh38
NC_000002.11:g.62054395T>A , CM000664.1:g.62054395T>A	GRCh37
NC_000002.10:g.61907899T>A	NCBI36
NG_028125.1:g.31884A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1852-2A>T MANE Select	NP_001188472.1:n.1852-2A>T
ENST00000404929.6:c.1852-2A>T MANE Select	ENSP00000385158.1:n.1852-2A>T
NM_001201543.1:c.1852-2A>T	NP_001188472.1:n.1852-2A>T
NM_032180.2:c.1684-2A>T	NP_115556.2:n.1684-2A>T
NM_032180.3:c.1684-2A>T	NP_115556.2:n.1684-2A>T
NR_037710.1:n.1730-2A>T
NR_037710.2:n.1647-2A>T
ENST00000404929.5:c.1852-2A>T	ENSP00000385158.1:n.1852-2A>T
ENST00000405894.3:c.1684-2A>T	ENSP00000385893.3:n.1684-2A>T
ENST00000418113.5:c.2129-2A>T
ENST00000456262.5:c.*1199-2A>T	ENSP00000396105.1:n.*1199-2A>T
ENST00000478494.1:n.476-2A>T
XM_017005072.1:c.1357-2A>T	XP_016860561.1:n.1357-2A>T
XM_017005073.1:c.1282-2A>T	XP_016860562.1:n.1282-2A>T
XM_017005074.1:c.1114-2A>T	XP_016860563.1:n.1114-2A>T
XR_001738972.2:n.1853-2A>T
XR_001738973.2:n.1685-2A>T
XR_001738974.2:n.1853-2A>T
XR_001738976.1:n.1881-2A>T
XR_001738977.1:n.1713-2A>T
XR_939724.1:n.3213-2A>T