Canonical Allele Identifier: CA1132721992
Gene: FUNDC1 HGNC NCBI

Linked Data

gnomAD v3: X-44540990-ATGGCATTTGC-A
gnomAD v4: X-44540990-ATGGCATTTGC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540991_44541000del , CM000685.2:g.44540991_44541000del GRCh38
NC_000023.10:g.44400237_44400246del , CM000685.1:g.44400237_44400246del GRCh37
NC_000023.9:g.44285181_44285190del NCBI36
NG_021288.1:g.6976_6985del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+945_185+954del MANE Select ENSP00000367284.4:n.185+945_185+954del
ENST00000378045.4:c.185+945_185+954del ENSP00000367284.4:n.185+945_185+954del
ENST00000483115.1:n.360+945_360+954del
NM_173794.3:c.185+945_185+954del NP_776155.1:n.185+945_185+954del
NM_173794.4:c.185+945_185+954del MANE Select NP_776155.1:n.185+945_185+954del
Search 100 bp 5'
Search 100 bp 3'