Canonical Allele Identifier: CA329528450
Gene: FUNDC1 HGNC NCBI

Linked Data

dbSNP Id: rs758000896
MyVariant Identifiers: chrX:g.44400189_44400190insC (hg19) chrX:g.44540943_44540944insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.44540944dup , CM000685.2:g.44540944dup GRCh38
NC_000023.10:g.44400190dup , CM000685.1:g.44400190dup GRCh37
NC_000023.9:g.44285134dup NCBI36
NG_021288.1:g.7032dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000378045.5:c.185+1001dup MANE Select ENSP00000367284.4:n.185+1001dup
ENST00000378045.4:c.185+1001dup ENSP00000367284.4:n.185+1001dup
ENST00000483115.1:n.360+1001dup
NM_173794.3:c.185+1001dup NP_776155.1:n.185+1001dup
NM_173794.4:c.185+1001dup MANE Select NP_776155.1:n.185+1001dup
Search 100 bp 5'
Search 100 bp 3'