Canonical Allele Identifier: CA346989361

Gene: FAM161A

Linked Data

• MyVariant Identifiers: chr2:g.62069325C>G (hg19) ; chr2:g.61842190C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.61842190C>G , CM000664.2:g.61842190C>G	GRCh38
NC_000002.11:g.62069325C>G , CM000664.1:g.62069325C>G	GRCh37
NC_000002.10:g.61922829C>G	NCBI36
NG_028125.1:g.16954G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000404929.6:c.354G>C MANE Select	ENSP00000385158.1:p.Gln118His
ENST00000307507.3:c.*364G>C	ENSP00000303170.3:n.*364G>C
ENST00000404929.5:c.354G>C	ENSP00000385158.1:p.Gln118His
ENST00000405894.3:c.354G>C	ENSP00000385893.3:p.Gln118His
ENST00000418113.5:c.341G>C
ENST00000456262.5:c.354G>C	ENSP00000396105.1:p.Gln118His
NM_001201543.1:c.354G>C	NP_001188472.1:p.Gln118His
NM_032180.2:c.354G>C	NP_115556.2:p.Gln118His
NR_037710.1:n.456G>C
XR_939724.1:n.1715G>C
XM_017005072.1:c.27G>C	XP_016860561.1:p.Gln9His
XM_017005073.1:c.-161G>C	XP_016860562.1:n.-161G>C
XM_017005074.1:c.-161G>C	XP_016860563.1:n.-161G>C
XR_001738972.2:n.355G>C
XR_001738973.2:n.355G>C
XR_001738974.2:n.355G>C
XR_001738975.2:n.355G>C
XR_001738976.1:n.439G>C
XR_001738977.1:n.439G>C
NM_001201543.2:c.354G>C MANE Select	NP_001188472.1:p.Gln118His
NM_032180.3:c.354G>C	NP_115556.2:p.Gln118His
NR_037710.2:n.373G>C