Canonical Allele Identifier: CA2426939916
Gene: FUNDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540879C= , CM000685.2:g.44540879C= GRCh38
NC_000023.10:g.44400125C= , CM000685.1:g.44400125C= GRCh37
NC_000023.9:g.44285069C= NCBI36
NG_021288.1:g.7097G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+1066G= MANE Select ENSP00000367284.4:n.185+1066G=
ENST00000378045.4:c.185+1066G= ENSP00000367284.4:n.185+1066G=
ENST00000483115.1:n.360+1066G=
NM_173794.3:c.185+1066G= NP_776155.1:n.185+1066G=
NM_173794.4:c.185+1066G= MANE Select NP_776155.1:n.185+1066G=