Canonical Allele Identifier: CA2640697885
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727578-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727578G>T , CM000679.2:g.82727578G>T GRCh38
NC_000017.10:g.80685454G>T , CM000679.1:g.80685454G>T GRCh37
NC_000017.9:g.78278743G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*407G>T MANE Select ENSP00000269373.6:n.*407G>T
ENST00000269373.10:c.*407G>T ENSP00000269373.6:n.*407G>T
ENST00000571594.1:c.53+411G>T ENSP00000459751.1:n.53+411G>T
NM_024619.3:c.*407G>T NP_078895.2:n.*407G>T
NR_046408.1:n.1515G>T
XM_024450948.1:c.*407G>T XP_024306716.1:n.*407G>T
NM_024619.4:c.*407G>T MANE Select NP_078895.2:n.*407G>T
NR_046408.2:n.1515G>T
Search 100 bp 5'
Search 100 bp 3'