Canonical Allele Identifier: CA236687435

Gene: FAIM2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49898003C>T , CM000674.2:g.49898003C>T	GRCh38
NC_000012.11:g.50291786C>T , CM000674.1:g.50291786C>T	GRCh37
NC_000012.10:g.48578053C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_012306.4:c.299G>A MANE Select	NP_036438.2:p.Arg100Gln
ENST00000320634.8:c.299G>A MANE Select	ENSP00000321951.3:p.Arg100Gln
NM_012306.3:c.299G>A	NP_036438.2:p.Arg100Gln
ENST00000320634.7:c.299G>A	ENSP00000321951.3:p.Arg100Gln
ENST00000547871.1:c.161G>A	ENSP00000449360.1:p.Arg54Gln
ENST00000550195.5:c.299G>A	ENSP00000447715.1:p.Arg100Gln
ENST00000550635.6:c.299G>A	ENSP00000449711.2:p.Arg100Gln
ENST00000550890.5:c.161G>A	ENSP00000450132.1:p.Arg54Gln
ENST00000552669.5:c.173G>A	ENSP00000446771.1:p.Arg58Gln
XM_005268730.2:c.173G>A	XP_005268787.1:p.Arg58Gln
XM_005268730.3:c.173G>A	XP_005268787.1:p.Arg58Gln