Canonical Allele Identifier: CA346990009

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61853972C>A , CM000664.2:g.61853972C>A	GRCh38
NC_000002.11:g.62081107C>A , CM000664.1:g.62081107C>A	GRCh37
NC_000002.10:g.61934611C>A	NCBI36
NG_028125.1:g.5172G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.70G>T MANE Select	NP_001188472.1:p.Gly24Ter
ENST00000404929.6:c.70G>T MANE Select	ENSP00000385158.1:p.Gly24Ter
NM_001201543.1:c.70G>T	NP_001188472.1:p.Gly24Ter
NM_032180.2:c.70G>T	NP_115556.2:p.Gly24Ter
NM_032180.3:c.70G>T	NP_115556.2:p.Gly24Ter
NR_037710.1:n.172G>T
NR_037710.2:n.89G>T
ENST00000307507.3:c.70G>T	ENSP00000303170.3:p.Gly24Ter
ENST00000404929.5:c.70G>T	ENSP00000385158.1:p.Gly24Ter
ENST00000405894.3:c.70G>T	ENSP00000385893.3:p.Gly24Ter
ENST00000418113.5:c.57G>T
ENST00000456262.5:c.70G>T	ENSP00000396105.1:p.Gly24Ter
XM_017005073.1:c.-445G>T	XP_016860562.1:n.-445G>T
XR_001738972.2:n.71G>T
XR_001738973.2:n.71G>T
XR_001738974.2:n.71G>T
XR_001738975.2:n.71G>T
XR_001738976.1:n.155G>T
XR_001738977.1:n.155G>T
XR_939724.1:n.1431G>T