Canonical Allele Identifier: CA2279173877
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1598336712

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727309C>T , CM000679.2:g.82727309C>T GRCh38
NC_000017.10:g.80685185C>T , CM000679.1:g.80685185C>T GRCh37
NC_000017.9:g.78278474C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*138C>T MANE Select ENSP00000269373.6:n.*138C>T
ENST00000269373.10:c.*138C>T ENSP00000269373.6:n.*138C>T
ENST00000571594.1:c.53+142C>T ENSP00000459751.1:n.53+142C>T
ENST00000574832.5:c.*1025C>T ENSP00000460869.1:n.*1025C>T
NM_024619.3:c.*138C>T NP_078895.2:n.*138C>T
NR_046408.1:n.1246C>T
XM_024450948.1:c.*138C>T XP_024306716.1:n.*138C>T
NM_024619.4:c.*138C>T MANE Select NP_078895.2:n.*138C>T
NR_046408.2:n.1246C>T