Canonical Allele Identifier: CA735103048

Gene: FNDC5

Linked Data

• dbSNP Id: rs1746661
• gnomAD v3: 1-32869438-G-A
• gnomAD v4: 1-32869438-G-A
• MyVariant Identifiers: chr1:g.33335039G>A (hg19) ; chr1:g.32869438G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.32869438G>A , CM000663.2:g.32869438G>A	GRCh38
NC_000001.10:g.33335039G>A , CM000663.1:g.33335039G>A	GRCh37
NC_000001.9:g.33107626G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000710568.1:c.239-441C>T	ENSP00000518350.1:n.239-441C>T
ENST00000373471.9:c.95-441C>T MANE Select	ENSP00000362570.5:n.95-441C>T
ENST00000649537.2:c.95-441C>T	ENSP00000497837.2:n.95-441C>T
ENST00000373471.7:c.95-441C>T	ENSP00000362570.4:n.95-441C>T
ENST00000496770.1:c.-127-445C>T	ENSP00000476320.1:n.-127-445C>T
NM_001171940.1:c.95-441C>T	NP_001165411.2:n.95-441C>T
NM_001171941.2:c.-127-445C>T	NP_001165412.1:n.-127-445C>T
NM_153756.2:c.95-441C>T	NP_715637.2:n.95-441C>T
NM_153756.3:c.95-441C>T MANE Select	NP_715637.2:n.95-441C>T
NM_001171940.2:c.95-441C>T	NP_001165411.2:n.95-441C>T
NM_001171941.3:c.-127-445C>T	NP_001165412.1:n.-127-445C>T