Canonical Allele Identifier: CA345717574

Gene: FAM110C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.45696C>A , CM000664.2:g.45696C>A	GRCh38
NC_000002.11:g.45696C>A , CM000664.1:g.45696C>A	GRCh37
NC_000002.10:g.35696C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001077710.3:c.690G>T MANE Select	NP_001071178.2:p.Glu230Asp
ENST00000327669.5:c.690G>T MANE Select	ENSP00000328347.4:p.Glu230Asp
NM_001077710.2:c.690G>T	NP_001071178.2:p.Glu230Asp
ENST00000327669.4:c.690G>T	ENSP00000328347.4:p.Glu230Asp
ENST00000461026.1:n.64+1111G>T
XM_011510372.1:c.690G>T	XP_011508674.1:p.Glu230Asp
XM_011510372.2:c.690G>T	XP_011508674.1:p.Glu230Asp
XM_011510373.1:c.690G>T	XP_011508675.1:p.Glu230Asp
XM_011510374.1:c.690G>T	XP_011508676.1:p.Glu230Asp
XM_017004689.1:c.690G>T	XP_016860178.1:p.Glu230Asp
XM_017004690.1:c.690G>T	XP_016860179.1:p.Glu230Asp
XM_017004691.1:c.690G>T	XP_016860180.1:p.Glu230Asp
XM_017004692.1:c.690G>T	XP_016860181.1:p.Glu230Asp
XR_001738890.1:n.895G>T