Canonical Allele Identifier: CA346987033

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61839799G>C , CM000664.2:g.61839799G>C	GRCh38
NC_000002.11:g.62066934G>C , CM000664.1:g.62066934G>C	GRCh37
NC_000002.10:g.61920438G>C	NCBI36
NG_028125.1:g.19345C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1205C>G MANE Select	NP_001188472.1:p.Ser402Ter
ENST00000404929.6:c.1205C>G MANE Select	ENSP00000385158.1:p.Ser402Ter
NM_001201543.1:c.1205C>G	NP_001188472.1:p.Ser402Ter
NM_032180.2:c.1205C>G	NP_115556.2:p.Ser402Ter
NM_032180.3:c.1205C>G	NP_115556.2:p.Ser402Ter
NR_037710.1:n.1251C>G
NR_037710.2:n.1168C>G
ENST00000307507.3:c.*1215C>G	ENSP00000303170.3:n.*1215C>G
ENST00000404929.5:c.1205C>G	ENSP00000385158.1:p.Ser402Ter
ENST00000405894.3:c.1205C>G	ENSP00000385893.3:p.Ser402Ter
ENST00000418113.5:c.1192C>G
ENST00000456262.5:c.*720C>G	ENSP00000396105.1:n.*720C>G
XM_017005072.1:c.878C>G	XP_016860561.1:p.Ser293Ter
XM_017005073.1:c.635C>G	XP_016860562.1:p.Ser212Ter
XM_017005074.1:c.635C>G	XP_016860563.1:p.Ser212Ter
XR_001738972.2:n.1206C>G
XR_001738973.2:n.1206C>G
XR_001738974.2:n.1206C>G
XR_001738975.2:n.1206C>G
XR_001738976.1:n.1234C>G
XR_001738977.1:n.1234C>G
XR_939724.1:n.2566C>G