Canonical Allele Identifier: CA1826275735

Gene: FBXL6 SLC52A2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.144358205G= , CM000670.2:g.144358205G=	GRCh38
NC_000008.10:g.145581865G= , CM000670.1:g.145581865G=	GRCh37
NC_000008.9:g.145552673G=	NCBI36
NG_032872.1:g.4649G=
NG_032872.2:g.4649G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331890.6:c.243C= (FBXL6) MANE Select	ENSP00000330098.5:p.Pro81=
ENST00000532815.2:c.-111+603G= (SLC52A2)	ENSP00000501933.1:n.-111+603G=
ENST00000675292.1:c.-110-979G= (SLC52A2)	ENSP00000502652.1:n.-110-979G=
ENST00000675888.1:c.-110-979G= (SLC52A2)	ENSP00000502294.1:n.-110-979G=
ENST00000331890.5:c.243C= (FBXL6)	ENSP00000330098.5:p.Pro81=
ENST00000455319.6:c.243C= (FBXL6)	ENSP00000403873.2:p.Pro81=
ENST00000524541.5:c.-110-979G= (SLC52A2)	ENSP00000434239.1:n.-110-979G=
ENST00000530142.5:n.1069C= (FBXL6)
ENST00000532815.1:n.399+603G= (SLC52A2)
NM_012162.3:c.243C= (FBXL6)	NP_036294.2:p.Pro81=
NM_024555.5:c.243C= (FBXL6)	NP_078831.4:p.Pro81=
NM_012162.4:c.243C= (FBXL6) MANE Select	NP_036294.2:p.Pro81=
NM_024555.6:c.243C= (FBXL6)	NP_078831.4:p.Pro81=