Canonical Allele Identifier: CA875592765
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs1431284720
MyVariant Identifiers: chrX:g.44400311_44400312del (hg19) chrX:g.44541065_44541066del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44541066_44541067del , CM000685.2:g.44541066_44541067del GRCh38
NC_000023.10:g.44400312_44400313del , CM000685.1:g.44400312_44400313del GRCh37
NC_000023.9:g.44285256_44285257del NCBI36
NG_021288.1:g.6910_6911del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+879_185+880del MANE Select ENSP00000367284.4:n.185+879_185+880del
ENST00000378045.4:c.185+879_185+880del ENSP00000367284.4:n.185+879_185+880del
ENST00000483115.1:n.360+879_360+880del
NM_173794.3:c.185+879_185+880del NP_776155.1:n.185+879_185+880del
NM_173794.4:c.185+879_185+880del MANE Select NP_776155.1:n.185+879_185+880del
Search 100 bp 5'
Search 100 bp 3'