Canonical Allele Identifier: CA1255593723

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61839695T= , CM000664.2:g.61839695T=	GRCh38
NC_000002.11:g.62066830T= , CM000664.1:g.62066830T=	GRCh37
NC_000002.10:g.61920334T=	NCBI36
NG_028125.1:g.19449A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404929.6:c.1309A= MANE Select	ENSP00000385158.1:p.Arg437=
ENST00000307507.3:c.*1319A=	ENSP00000303170.3:n.*1319A=
ENST00000404929.5:c.1309A=	ENSP00000385158.1:p.Arg437=
ENST00000405894.3:c.1309A=	ENSP00000385893.3:p.Arg437=
ENST00000418113.5:c.1296A=
ENST00000456262.5:c.*824A=	ENSP00000396105.1:n.*824A=
NM_001201543.1:c.1309A=	NP_001188472.1:p.Arg437=
NM_032180.2:c.1309A=	NP_115556.2:p.Arg437=
NR_037710.1:n.1355A=
XR_939724.1:n.2670A=
XM_017005072.1:c.982A=	XP_016860561.1:p.Arg328=
XM_017005073.1:c.739A=	XP_016860562.1:p.Arg247=
XM_017005074.1:c.739A=	XP_016860563.1:p.Arg247=
XR_001738972.2:n.1310A=
XR_001738973.2:n.1310A=
XR_001738974.2:n.1310A=
XR_001738975.2:n.1310A=
XR_001738976.1:n.1338A=
XR_001738977.1:n.1338A=
NM_001201543.2:c.1309A= MANE Select	NP_001188472.1:p.Arg437=
NM_032180.3:c.1309A=	NP_115556.2:p.Arg437=
NR_037710.2:n.1272A=