Canonical Allele Identifier: CA2426939918
Gene: FUNDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540883T= , CM000685.2:g.44540883T= GRCh38
NC_000023.10:g.44400129T= , CM000685.1:g.44400129T= GRCh37
NC_000023.9:g.44285073T= NCBI36
NG_021288.1:g.7093A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+1062A= MANE Select ENSP00000367284.4:n.185+1062A=
ENST00000378045.4:c.185+1062A= ENSP00000367284.4:n.185+1062A=
ENST00000483115.1:n.360+1062A=
NM_173794.3:c.185+1062A= NP_776155.1:n.185+1062A=
NM_173794.4:c.185+1062A= MANE Select NP_776155.1:n.185+1062A=