Canonical Allele Identifier: CA2640697425
Gene: FN3KRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727454A>G , CM000679.2:g.82727454A>G GRCh38
NC_000017.10:g.80685330A>G , CM000679.1:g.80685330A>G GRCh37
NC_000017.9:g.78278619A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*283A>G MANE Select ENSP00000269373.6:n.*283A>G
ENST00000269373.10:c.*283A>G ENSP00000269373.6:n.*283A>G
ENST00000571594.1:c.53+287A>G ENSP00000459751.1:n.53+287A>G
ENST00000574832.5:c.*1170A>G ENSP00000460869.1:n.*1170A>G
NM_024619.3:c.*283A>G NP_078895.2:n.*283A>G
NR_046408.1:n.1391A>G
XM_024450948.1:c.*283A>G XP_024306716.1:n.*283A>G
NM_024619.4:c.*283A>G MANE Select NP_078895.2:n.*283A>G
NR_046408.2:n.1391A>G