Canonical Allele Identifier: CA372624046
Gene: FBXL6 HGNC NCBI
SLC52A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.144358300A>C , CM000670.2:g.144358300A>C GRCh38
NC_000008.10:g.145581960A>C , CM000670.1:g.145581960A>C GRCh37
NC_000008.9:g.145552768A>C NCBI36
NG_032872.1:g.4744A>C
NG_032872.2:g.4744A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331890.6:c.148T>G (FBXL6) MANE Select ENSP00000330098.5:p.Ser50Ala
ENST00000532815.2:c.-111+698A>C (SLC52A2) ENSP00000501933.1:n.-111+698A>C
ENST00000675292.1:c.-110-884A>C (SLC52A2) ENSP00000502652.1:n.-110-884A>C
ENST00000675888.1:c.-110-884A>C (SLC52A2) ENSP00000502294.1:n.-110-884A>C
ENST00000331890.5:c.148T>G (FBXL6) ENSP00000330098.5:p.Ser50Ala
ENST00000455319.6:c.148T>G (FBXL6) ENSP00000403873.2:p.Ser50Ala
ENST00000524541.5:c.-110-884A>C (SLC52A2) ENSP00000434239.1:n.-110-884A>C
ENST00000530142.5:n.974T>G (FBXL6)
ENST00000532815.1:n.399+698A>C (SLC52A2)
NM_012162.3:c.148T>G (FBXL6) NP_036294.2:p.Ser50Ala
NM_024555.5:c.148T>G (FBXL6) NP_078831.4:p.Ser50Ala
NM_012162.4:c.148T>G (FBXL6) MANE Select NP_036294.2:p.Ser50Ala
NM_024555.6:c.148T>G (FBXL6) NP_078831.4:p.Ser50Ala