Canonical Allele Identifier: CA13098973

Gene: FAM120A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93526949G>A , CM000671.2:g.93526949G>A	GRCh38
NC_000009.11:g.96289231G>A , CM000671.1:g.96289231G>A	GRCh37
NC_000009.10:g.95329052G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014612.5:c.1419-206G>A MANE Select	NP_055427.2:n.1419-206G>A
ENST00000277165.11:c.1419-206G>A MANE Select	ENSP00000277165.5:n.1419-206G>A
NM_001286722.1:c.1416-206G>A	NP_001273651.1:n.1416-206G>A
NM_001286722.2:c.1416-206G>A	NP_001273651.1:n.1416-206G>A
NM_001286723.1:c.1419-206G>A	NP_001273652.1:n.1419-206G>A
NM_001286723.2:c.1419-206G>A	NP_001273652.1:n.1419-206G>A
NM_001286724.1:c.1419-206G>A	NP_001273653.1:n.1419-206G>A
NM_001286724.2:c.1419-206G>A	NP_001273653.1:n.1419-206G>A
NM_014612.4:c.1419-206G>A	NP_055427.2:n.1419-206G>A
ENST00000277165.10:c.1419-206G>A	ENSP00000277165.5:n.1419-206G>A
ENST00000375389.7:c.1419-206G>A	ENSP00000364538.3:n.1419-206G>A
ENST00000446420.2:c.951-206G>A	ENSP00000396534.2:n.951-206G>A
ENST00000698944.1:c.1419-206G>A	ENSP00000514050.1:n.1419-206G>A
XM_005251842.3:c.1419-206G>A	XP_005251899.1:n.1419-206G>A
XM_005251842.5:c.1419-206G>A	XP_005251899.1:n.1419-206G>A
XM_011518412.1:c.1503-206G>A	XP_011516714.1:n.1503-206G>A
XM_011518412.2:c.1503-206G>A	XP_011516714.1:n.1503-206G>A
XM_011518413.1:c.1503-206G>A	XP_011516715.1:n.1503-206G>A
XM_011518413.2:c.1503-206G>A	XP_011516715.1:n.1503-206G>A
XM_011518414.1:c.1500-206G>A	XP_011516716.1:n.1500-206G>A
XM_011518414.3:c.1500-206G>A	XP_011516716.1:n.1500-206G>A
XM_011518415.1:c.1503-206G>A	XP_011516717.1:n.1503-206G>A
XM_011518416.1:c.1503-206G>A	XP_011516718.1:n.1503-206G>A
XM_011518416.3:c.1503-206G>A	XP_011516718.1:n.1503-206G>A