Canonical Allele Identifier: CA1679227

Gene: FAM161A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61839960A>G , CM000664.2:g.61839960A>G	GRCh38
NC_000002.11:g.62067095A>G , CM000664.1:g.62067095A>G	GRCh37
NC_000002.10:g.61920599A>G	NCBI36
NG_028125.1:g.19184T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001201543.2:c.1044T>C MANE Select	NP_001188472.1:p.Tyr348=
ENST00000404929.6:c.1044T>C MANE Select	ENSP00000385158.1:p.Tyr348=
NM_001201543.1:c.1044T>C	NP_001188472.1:p.Tyr348=
NM_032180.2:c.1044T>C	NP_115556.2:p.Tyr348=
NM_032180.3:c.1044T>C	NP_115556.2:p.Tyr348=
NR_037710.1:n.1090T>C
NR_037710.2:n.1007T>C
ENST00000307507.3:c.*1054T>C	ENSP00000303170.3:n.*1054T>C
ENST00000404929.5:c.1044T>C	ENSP00000385158.1:p.Tyr348=
ENST00000405894.3:c.1044T>C	ENSP00000385893.3:p.Tyr348=
ENST00000418113.5:c.1031T>C
ENST00000456262.5:c.*559T>C	ENSP00000396105.1:n.*559T>C
XM_017005072.1:c.717T>C	XP_016860561.1:p.Tyr239=
XM_017005073.1:c.474T>C	XP_016860562.1:p.Tyr158=
XM_017005074.1:c.474T>C	XP_016860563.1:p.Tyr158=
XR_001738972.2:n.1045T>C
XR_001738973.2:n.1045T>C
XR_001738974.2:n.1045T>C
XR_001738975.2:n.1045T>C
XR_001738976.1:n.1073T>C
XR_001738977.1:n.1073T>C
XR_939724.1:n.2405T>C