Canonical Allele Identifier: CA8850997
Gene: FASN HGNC NCBI

Linked Data

ClinVar Variation Id: 2781123
ClinVar RCV Id: RCV003755109
dbSNP Id: rs754847679

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82079294G>A , CM000679.2:g.82079294G>A GRCh38
NC_000017.10:g.80037170G>A , CM000679.1:g.80037170G>A GRCh37
NC_000017.9:g.77630459G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306749.4:c.7399-14C>T MANE Select ENSP00000304592.2:n.7399-14C>T
ENST00000636628.1:c.28C>T
ENST00000306749.3:c.7399-14C>T ENSP00000304592.2:n.7399-14C>T
ENST00000578424.2:n.678-14C>T
ENST00000580382.1:c.569-14C>T
ENST00000584610.2:n.574-14C>T
ENST00000634990.1:c.7393-14C>T ENSP00000488964.1:n.7393-14C>T
NM_004104.4:c.7399-14C>T NP_004095.4:n.7399-14C>T
XM_011523538.1:c.7399-14C>T XP_011521840.1:n.7399-14C>T
XM_011523538.2:c.7399-14C>T XP_011521840.1:n.7399-14C>T
NM_004104.5:c.7399-14C>T MANE Select NP_004095.4:n.7399-14C>T