Canonical Allele Identifier: CA627824859
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1252039663
gnomAD v2: 17-80685814-CAT-C
gnomAD v3: 17-82727938-CAT-C
gnomAD v4: 17-82727938-CAT-C
MyVariant Identifiers: chr17:g.80685815_80685816del (hg19) chr17:g.82727939_82727940del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727941_82727942del , CM000679.2:g.82727941_82727942del GRCh38
NC_000017.10:g.80685817_80685818del , CM000679.1:g.80685817_80685818del GRCh37
NC_000017.9:g.78279106_78279107del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*770_*771del MANE Select ENSP00000269373.6:n.*770_*771del
ENST00000269373.10:c.*770_*771del ENSP00000269373.6:n.*770_*771del
ENST00000571594.1:c.53+774_53+775del ENSP00000459751.1:n.53+774_53+775del
NM_024619.3:c.*770_*771del NP_078895.2:n.*770_*771del
NR_046408.1:n.1878_1879del
XM_024450948.1:c.*770_*771del XP_024306716.1:n.*770_*771del
NM_024619.4:c.*770_*771del MANE Select NP_078895.2:n.*770_*771del
NR_046408.2:n.1878_1879del
Search 100 bp 5'
Search 100 bp 3'