Canonical Allele Identifier: CA2820675367
Gene: FUNDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540952_44540953insG , CM000685.2:g.44540952_44540953insG GRCh38
NC_000023.10:g.44400198_44400199insG , CM000685.1:g.44400198_44400199insG GRCh37
NC_000023.9:g.44285142_44285143insG NCBI36
NG_021288.1:g.7023_7024insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+992_185+993insC MANE Select ENSP00000367284.4:n.185+992_185+993insC
ENST00000378045.4:c.185+992_185+993insC ENSP00000367284.4:n.185+992_185+993insC
ENST00000483115.1:n.360+992_360+993insC
NM_173794.3:c.185+992_185+993insC NP_776155.1:n.185+992_185+993insC
NM_173794.4:c.185+992_185+993insC MANE Select NP_776155.1:n.185+992_185+993insC