Canonical Allele Identifier: CA346985613

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61836012G>A , CM000664.2:g.61836012G>A	GRCh38
NC_000002.11:g.62063147G>A , CM000664.1:g.62063147G>A	GRCh37
NC_000002.10:g.61916651G>A	NCBI36
NG_028125.1:g.23132C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1849C>T MANE Select	NP_001188472.1:p.Gln617Ter
ENST00000404929.6:c.1849C>T MANE Select	ENSP00000385158.1:p.Gln617Ter
NM_001201543.1:c.1849C>T	NP_001188472.1:p.Gln617Ter
NM_032180.2:c.1681C>T	NP_115556.2:p.Gln561Ter
NM_032180.3:c.1681C>T	NP_115556.2:p.Gln561Ter
NR_037710.1:n.1727C>T
NR_037710.2:n.1644C>T
ENST00000404929.5:c.1849C>T	ENSP00000385158.1:p.Gln617Ter
ENST00000405894.3:c.1681C>T	ENSP00000385893.3:p.Gln561Ter
ENST00000418113.5:c.2126C>T
ENST00000456262.5:c.*1196C>T	ENSP00000396105.1:n.*1196C>T
ENST00000478494.1:n.473C>T
ENST00000496369.1:n.202C>T
XM_017005072.1:c.1354C>T	XP_016860561.1:p.Gln452Ter
XM_017005073.1:c.1279C>T	XP_016860562.1:p.Gln427Ter
XM_017005074.1:c.1111C>T	XP_016860563.1:p.Gln371Ter
XR_001738972.2:n.1850C>T
XR_001738973.2:n.1682C>T
XR_001738974.2:n.1850C>T
XR_001738976.1:n.1878C>T
XR_001738977.1:n.1710C>T
XR_939724.1:n.3210C>T