Canonical Allele Identifier: CA346986221

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61838707T>C , CM000664.2:g.61838707T>C	GRCh38
NC_000002.11:g.62065842T>C , CM000664.1:g.62065842T>C	GRCh37
NC_000002.10:g.61919346T>C	NCBI36
NG_028125.1:g.20437A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1584-2A>G MANE Select	NP_001188472.1:n.1584-2A>G
ENST00000404929.6:c.1584-2A>G MANE Select	ENSP00000385158.1:n.1584-2A>G
NM_001201543.1:c.1584-2A>G	NP_001188472.1:n.1584-2A>G
NM_032180.2:c.1583+714A>G	NP_115556.2:n.1583+714A>G
NM_032180.3:c.1583+714A>G	NP_115556.2:n.1583+714A>G
NR_037710.1:n.1629+714A>G
NR_037710.2:n.1546+714A>G
ENST00000307507.3:c.*1593+714A>G	ENSP00000303170.3:n.*1593+714A>G
ENST00000404929.5:c.1584-2A>G	ENSP00000385158.1:n.1584-2A>G
ENST00000405894.3:c.1583+714A>G	ENSP00000385893.3:n.1583+714A>G
ENST00000418113.5:c.1571-2A>G
ENST00000456262.5:c.*1098+714A>G	ENSP00000396105.1:n.*1098+714A>G
ENST00000496369.1:n.104+714A>G
XM_017005072.1:c.1256+714A>G	XP_016860561.1:n.1256+714A>G
XM_017005073.1:c.1014-2A>G	XP_016860562.1:n.1014-2A>G
XM_017005074.1:c.1013+714A>G	XP_016860563.1:n.1013+714A>G
XR_001738972.2:n.1585-2A>G
XR_001738973.2:n.1584+714A>G
XR_001738974.2:n.1585-2A>G
XR_001738975.2:n.1585-2A>G
XR_001738976.1:n.1613-2A>G
XR_001738977.1:n.1612+714A>G
XR_939724.1:n.2945-2A>G