Canonical Allele Identifier: CA2640697919
Gene: FN3KRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727594T>C , CM000679.2:g.82727594T>C GRCh38
NC_000017.10:g.80685470T>C , CM000679.1:g.80685470T>C GRCh37
NC_000017.9:g.78278759T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*423T>C MANE Select ENSP00000269373.6:n.*423T>C
ENST00000269373.10:c.*423T>C ENSP00000269373.6:n.*423T>C
ENST00000571594.1:c.53+427T>C ENSP00000459751.1:n.53+427T>C
NM_024619.3:c.*423T>C NP_078895.2:n.*423T>C
NR_046408.1:n.1531T>C
XM_024450948.1:c.*423T>C XP_024306716.1:n.*423T>C
NM_024619.4:c.*423T>C MANE Select NP_078895.2:n.*423T>C
NR_046408.2:n.1531T>C