Canonical Allele Identifier: CA295269609
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs892787544
gnomAD v4: 17-82727440-C-A
MyVariant Identifiers: chr17:g.80685316C>A (hg19) chr17:g.82727440C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727440C>A , CM000679.2:g.82727440C>A GRCh38
NC_000017.10:g.80685316C>A , CM000679.1:g.80685316C>A GRCh37
NC_000017.9:g.78278605C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*269C>A MANE Select ENSP00000269373.6:n.*269C>A
ENST00000269373.10:c.*269C>A ENSP00000269373.6:n.*269C>A
ENST00000571594.1:c.53+273C>A ENSP00000459751.1:n.53+273C>A
ENST00000574832.5:c.*1156C>A ENSP00000460869.1:n.*1156C>A
NM_024619.3:c.*269C>A NP_078895.2:n.*269C>A
NR_046408.1:n.1377C>A
XM_024450948.1:c.*269C>A XP_024306716.1:n.*269C>A
NM_024619.4:c.*269C>A MANE Select NP_078895.2:n.*269C>A
NR_046408.2:n.1377C>A
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