Canonical Allele Identifier: CA1679069

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61838623G>A , CM000664.2:g.61838623G>A	GRCh38
NC_000002.11:g.62065758G>A , CM000664.1:g.62065758G>A	GRCh37
NC_000002.10:g.61919262G>A	NCBI36
NG_028125.1:g.20521C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1666C>T MANE Select	NP_001188472.1:p.Gln556Ter
ENST00000404929.6:c.1666C>T MANE Select	ENSP00000385158.1:p.Gln556Ter
NM_001201543.1:c.1666C>T	NP_001188472.1:p.Gln556Ter
NM_032180.2:c.1583+798C>T	NP_115556.2:n.1583+798C>T
NM_032180.3:c.1583+798C>T	NP_115556.2:n.1583+798C>T
NR_037710.1:n.1629+798C>T
NR_037710.2:n.1546+798C>T
ENST00000307507.3:c.*1593+798C>T	ENSP00000303170.3:n.*1593+798C>T
ENST00000404929.5:c.1666C>T	ENSP00000385158.1:p.Gln556Ter
ENST00000405894.3:c.1583+798C>T	ENSP00000385893.3:n.1583+798C>T
ENST00000418113.5:c.1653C>T
ENST00000456262.5:c.*1098+798C>T	ENSP00000396105.1:n.*1098+798C>T
ENST00000496369.1:n.104+798C>T
XM_017005072.1:c.1256+798C>T	XP_016860561.1:n.1256+798C>T
XM_017005073.1:c.1096C>T	XP_016860562.1:p.Gln366Ter
XM_017005074.1:c.1013+798C>T	XP_016860563.1:n.1013+798C>T
XR_001738972.2:n.1667C>T
XR_001738973.2:n.1584+798C>T
XR_001738974.2:n.1667C>T
XR_001738975.2:n.1667C>T
XR_001738976.1:n.1695C>T
XR_001738977.1:n.1612+798C>T
XR_939724.1:n.3027C>T