Canonical Allele Identifier: CA426212420

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61853883T>C , CM000664.2:g.61853883T>C	GRCh38
NC_000002.11:g.62081018T>C , CM000664.1:g.62081018T>C	GRCh37
NC_000002.10:g.61934522T>C	NCBI36
NG_028125.1:g.5261A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.159A>G MANE Select	NP_001188472.1:p.Lys53=
ENST00000404929.6:c.159A>G MANE Select	ENSP00000385158.1:p.Lys53=
NM_001201543.1:c.159A>G	NP_001188472.1:p.Lys53=
NM_032180.2:c.159A>G	NP_115556.2:p.Lys53=
NM_032180.3:c.159A>G	NP_115556.2:p.Lys53=
NR_037710.1:n.261A>G
NR_037710.2:n.178A>G
ENST00000307507.3:c.159A>G	ENSP00000303170.3:p.Lys53=
ENST00000404929.5:c.159A>G	ENSP00000385158.1:p.Lys53=
ENST00000405894.3:c.159A>G	ENSP00000385893.3:p.Lys53=
ENST00000418113.5:c.146A>G
ENST00000456262.5:c.159A>G	ENSP00000396105.1:p.Lys53=
XM_017005073.1:c.-356A>G	XP_016860562.1:n.-356A>G
XR_001738972.2:n.160A>G
XR_001738973.2:n.160A>G
XR_001738974.2:n.160A>G
XR_001738975.2:n.160A>G
XR_001738976.1:n.244A>G
XR_001738977.1:n.244A>G
XR_939724.1:n.1520A>G