Canonical Allele Identifier: CA1679111

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61839410T>C , CM000664.2:g.61839410T>C	GRCh38
NC_000002.11:g.62066545T>C , CM000664.1:g.62066545T>C	GRCh37
NC_000002.10:g.61920049T>C	NCBI36
NG_028125.1:g.19734A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1583+11A>G MANE Select	NP_001188472.1:n.1583+11A>G
ENST00000404929.6:c.1583+11A>G MANE Select	ENSP00000385158.1:n.1583+11A>G
NM_001201543.1:c.1583+11A>G	NP_001188472.1:n.1583+11A>G
NM_032180.2:c.1583+11A>G	NP_115556.2:n.1583+11A>G
NM_032180.3:c.1583+11A>G	NP_115556.2:n.1583+11A>G
NR_037710.1:n.1629+11A>G
NR_037710.2:n.1546+11A>G
ENST00000307507.3:c.*1593+11A>G	ENSP00000303170.3:n.*1593+11A>G
ENST00000404929.5:c.1583+11A>G	ENSP00000385158.1:n.1583+11A>G
ENST00000405894.3:c.1583+11A>G	ENSP00000385893.3:n.1583+11A>G
ENST00000418113.5:c.1570+11A>G
ENST00000456262.5:c.*1098+11A>G	ENSP00000396105.1:n.*1098+11A>G
ENST00000496369.1:n.104+11A>G
XM_017005072.1:c.1256+11A>G	XP_016860561.1:n.1256+11A>G
XM_017005073.1:c.1013+11A>G	XP_016860562.1:n.1013+11A>G
XM_017005074.1:c.1013+11A>G	XP_016860563.1:n.1013+11A>G
XR_001738972.2:n.1584+11A>G
XR_001738973.2:n.1584+11A>G
XR_001738974.2:n.1584+11A>G
XR_001738975.2:n.1584+11A>G
XR_001738976.1:n.1612+11A>G
XR_001738977.1:n.1612+11A>G
XR_939724.1:n.2944+11A>G