Canonical Allele Identifier: CA346988586

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61840309C>T , CM000664.2:g.61840309C>T	GRCh38
NC_000002.11:g.62067444C>T , CM000664.1:g.62067444C>T	GRCh37
NC_000002.10:g.61920948C>T	NCBI36
NG_028125.1:g.18835G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.695G>A MANE Select	NP_001188472.1:p.Trp232Ter
ENST00000404929.6:c.695G>A MANE Select	ENSP00000385158.1:p.Trp232Ter
NM_001201543.1:c.695G>A	NP_001188472.1:p.Trp232Ter
NM_032180.2:c.695G>A	NP_115556.2:p.Trp232Ter
NM_032180.3:c.695G>A	NP_115556.2:p.Trp232Ter
NR_037710.1:n.741G>A
NR_037710.2:n.658G>A
ENST00000307507.3:c.*705G>A	ENSP00000303170.3:n.*705G>A
ENST00000404929.5:c.695G>A	ENSP00000385158.1:p.Trp232Ter
ENST00000405894.3:c.695G>A	ENSP00000385893.3:p.Trp232Ter
ENST00000418113.5:c.682G>A
ENST00000456262.5:c.*210G>A	ENSP00000396105.1:n.*210G>A
XM_017005072.1:c.368G>A	XP_016860561.1:p.Trp123Ter
XM_017005073.1:c.125G>A	XP_016860562.1:p.Trp42Ter
XM_017005074.1:c.125G>A	XP_016860563.1:p.Trp42Ter
XR_001738972.2:n.696G>A
XR_001738973.2:n.696G>A
XR_001738974.2:n.696G>A
XR_001738975.2:n.696G>A
XR_001738976.1:n.724G>A
XR_001738977.1:n.724G>A
XR_939724.1:n.2056G>A