Canonical Allele Identifier: CA2640697879
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727575-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727575C>T , CM000679.2:g.82727575C>T GRCh38
NC_000017.10:g.80685451C>T , CM000679.1:g.80685451C>T GRCh37
NC_000017.9:g.78278740C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*404C>T MANE Select ENSP00000269373.6:n.*404C>T
ENST00000269373.10:c.*404C>T ENSP00000269373.6:n.*404C>T
ENST00000571594.1:c.53+408C>T ENSP00000459751.1:n.53+408C>T
NM_024619.3:c.*404C>T NP_078895.2:n.*404C>T
NR_046408.1:n.1512C>T
XM_024450948.1:c.*404C>T XP_024306716.1:n.*404C>T
NM_024619.4:c.*404C>T MANE Select NP_078895.2:n.*404C>T
NR_046408.2:n.1512C>T
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