Canonical Allele Identifier: CA4629569

Gene: FAM167A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11444390C>T , CM000670.2:g.11444390C>T	GRCh38
NC_000008.10:g.11301899C>T , CM000670.1:g.11301899C>T	GRCh37
NC_000008.9:g.11339309C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_053279.3:c.22G>A MANE Select	NP_444509.2:p.Val8Met
ENST00000284486.9:c.22G>A MANE Select	ENSP00000284486.4:p.Val8Met
NM_053279.2:c.22G>A	NP_444509.2:p.Val8Met
ENST00000284486.8:c.22G>A	ENSP00000284486.4:p.Val8Met
ENST00000527445.1:n.108-19754G>A
ENST00000528897.1:c.22G>A	ENSP00000436655.1:p.Val8Met
ENST00000531804.5:c.22G>A	ENSP00000431951.1:p.Val8Met
ENST00000534308.1:c.22G>A	ENSP00000432232.1:p.Val8Met
ENST00000648766.1:c.22G>A	ENSP00000497969.1:p.Val8Met
XM_005272398.3:c.22G>A	XP_005272455.1:p.Val8Met
XM_005272398.5:c.22G>A	XP_005272455.1:p.Val8Met
XM_011543837.1:c.22G>A	XP_011542139.1:p.Val8Met
XM_011543838.1:c.22G>A	XP_011542140.1:p.Val8Met
XM_011543838.3:c.22G>A	XP_011542140.1:p.Val8Met
XM_011543839.1:c.22G>A	XP_011542141.1:p.Val8Met
XM_011543840.1:c.22G>A	XP_011542142.1:p.Val8Met
XM_011543840.3:c.22G>A	XP_011542142.1:p.Val8Met
XM_024447292.1:c.22G>A	XP_024303060.1:p.Val8Met