Canonical Allele Identifier: CA348528300

Gene: FAM168B

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.131053010G>T , CM000664.2:g.131053010G>T	GRCh38
NC_000002.11:g.131810583G>T , CM000664.1:g.131810583G>T	GRCh37
NC_000002.10:g.131527053G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001009993.4:c.481C>A MANE Select	NP_001009993.2:p.Leu161Met
ENST00000389915.4:c.481C>A MANE Select	ENSP00000374565.3:p.Leu161Met
NM_001009993.2:c.481C>A	NP_001009993.2:p.Leu161Met
NM_001009993.3:c.481C>A	NP_001009993.2:p.Leu161Met
NM_001321743.1:c.481C>A	NP_001308672.1:p.Leu161Met
NM_001321744.1:c.481C>A	NP_001308673.1:p.Leu161Met
NM_001321745.1:c.481C>A	NP_001308674.1:p.Leu161Met
NM_001321746.1:c.481C>A	NP_001308675.1:p.Leu161Met
NM_001321746.2:c.481C>A	NP_001308675.1:p.Leu161Met
NM_001321747.1:c.481C>A	NP_001308676.1:p.Leu161Met
NM_001321747.2:c.481C>A	NP_001308676.1:p.Leu161Met
NM_001321748.1:c.481C>A	NP_001308677.1:p.Leu161Met
NM_001321748.2:c.481C>A	NP_001308677.1:p.Leu161Met
ENST00000389915.3:c.481C>A	ENSP00000374565.3:p.Leu161Met
ENST00000409185.5:c.481C>A	ENSP00000387051.1:p.Leu161Met
XM_005263591.3:c.481C>A	XP_005263648.1:p.Leu161Met
XM_006712263.2:c.481C>A	XP_006712326.1:p.Leu161Met
XM_006712264.2:c.481C>A	XP_006712327.1:p.Leu161Met
XM_006712265.2:c.481C>A	XP_006712328.1:p.Leu161Met
XM_011510593.1:c.481C>A	XP_011508895.1:p.Leu161Met
XM_011510594.1:c.400C>A	XP_011508896.1:p.Leu134Met
XM_011510594.3:c.400C>A	XP_011508896.1:p.Leu134Met
XM_017003327.1:c.481C>A	XP_016858816.1:p.Leu161Met
XM_017003328.1:c.400C>A	XP_016858817.1:p.Leu134Met