Canonical Allele Identifier: CA641658896
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs1314633923
gnomAD v2: X-44400246-CA-C
gnomAD v3: X-44541000-CA-C
gnomAD v4: X-44541000-CA-C
MyVariant Identifiers: chrX:g.44400247del (hg19) chrX:g.44541001del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44541009del , CM000685.2:g.44541009del GRCh38
NC_000023.10:g.44400255del , CM000685.1:g.44400255del GRCh37
NC_000023.9:g.44285199del NCBI36
NG_021288.1:g.6975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+944del MANE Select ENSP00000367284.4:n.185+944del
ENST00000378045.4:c.185+944del ENSP00000367284.4:n.185+944del
ENST00000483115.1:n.360+944del
NM_173794.3:c.185+944del NP_776155.1:n.185+944del
NM_173794.4:c.185+944del MANE Select NP_776155.1:n.185+944del
Search 100 bp 5'
Search 100 bp 3'