Canonical Allele Identifier: CA1550232

Gene: FAM228A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24190429A>G , CM000664.2:g.24190429A>G	GRCh38
NC_000002.11:g.24413298A>G , CM000664.1:g.24413298A>G	GRCh37
NC_000002.10:g.24266802A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432434.2:c.536A>G	ENSP00000412833.2:p.Tyr179Cys
ENST00000456591.6:c.*285A>G	ENSP00000401257.1:n.*285A>G
ENST00000295150.8:c.419A>G MANE Select	ENSP00000295150.3:p.Tyr140Cys
ENST00000295150.7:c.419A>G	ENSP00000295150.3:p.Tyr140Cys
ENST00000415196.1:c.122A>G	ENSP00000416595.1:p.Tyr41Cys
ENST00000432434.1:c.532A>G
ENST00000456591.5:c.*285A>G	ENSP00000401257.1:n.*285A>G
ENST00000610442.1:c.*1546A>G	ENSP00000483650.1:n.*1546A>G
NM_001040710.2:c.419A>G	NP_001035800.1:p.Tyr140Cys
NM_001040710.3:c.419A>G MANE Select	NP_001035800.1:p.Tyr140Cys