Canonical Allele Identifier: CA2640699534
Gene: FN3KRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727236G>T , CM000679.2:g.82727236G>T GRCh38
NC_000017.10:g.80685112G>T , CM000679.1:g.80685112G>T GRCh37
NC_000017.9:g.78278401G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*65G>T MANE Select ENSP00000269373.6:n.*65G>T
ENST00000269373.10:c.*65G>T ENSP00000269373.6:n.*65G>T
ENST00000571594.1:c.53+69G>T ENSP00000459751.1:n.53+69G>T
ENST00000574832.5:c.*952G>T ENSP00000460869.1:n.*952G>T
NM_024619.3:c.*65G>T NP_078895.2:n.*65G>T
NR_046408.1:n.1173G>T
XM_024450948.1:c.*65G>T XP_024306716.1:n.*65G>T
NM_024619.4:c.*65G>T MANE Select NP_078895.2:n.*65G>T
NR_046408.2:n.1173G>T