Canonical Allele Identifier: CA345717572
Community Standard Title: NM_001077710.3(FAM110C):c.691G>C (p.Ala231Pro)
Gene: FAM110C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.45695C>G , CM000664.2:g.45695C>G GRCh38
NC_000002.11:g.45695C>G , CM000664.1:g.45695C>G GRCh37
NC_000002.10:g.35695C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001077710.3:c.691G>C MANE Select NP_001071178.2:p.Ala231Pro
ENST00000327669.5:c.691G>C MANE Select ENSP00000328347.4:p.Ala231Pro
NM_001077710.2:c.691G>C NP_001071178.2:p.Ala231Pro
ENST00000327669.4:c.691G>C ENSP00000328347.4:p.Ala231Pro
ENST00000461026.1:n.64+1112G>C
XM_011510372.1:c.691G>C XP_011508674.1:p.Ala231Pro
XM_011510372.2:c.691G>C XP_011508674.1:p.Ala231Pro
XM_011510373.1:c.691G>C XP_011508675.1:p.Ala231Pro
XM_011510374.1:c.691G>C XP_011508676.1:p.Ala231Pro
XM_017004689.1:c.691G>C XP_016860178.1:p.Ala231Pro
XM_017004690.1:c.691G>C XP_016860179.1:p.Ala231Pro
XM_017004691.1:c.691G>C XP_016860180.1:p.Ala231Pro
XM_017004692.1:c.691G>C XP_016860181.1:p.Ala231Pro
XR_001738890.1:n.896G>C
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