Canonical Allele Identifier: CA2279173841
Gene: FN3KRP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727252G= , CM000679.2:g.82727252G= GRCh38
NC_000017.10:g.80685128G= , CM000679.1:g.80685128G= GRCh37
NC_000017.9:g.78278417G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*81G= MANE Select ENSP00000269373.6:n.*81G=
ENST00000269373.10:c.*81G= ENSP00000269373.6:n.*81G=
ENST00000571594.1:c.53+85G= ENSP00000459751.1:n.53+85G=
ENST00000574832.5:c.*968G= ENSP00000460869.1:n.*968G=
NM_024619.3:c.*81G= NP_078895.2:n.*81G=
NR_046408.1:n.1189G=
XM_024450948.1:c.*81G= XP_024306716.1:n.*81G=
NM_024619.4:c.*81G= MANE Select NP_078895.2:n.*81G=
NR_046408.2:n.1189G=
Search 100 bp 5'
Search 100 bp 3'