Canonical Allele Identifier: CA2640697288

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727379-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727379T>G , CM000679.2:g.82727379T>G	GRCh38
NC_000017.10:g.80685255T>G , CM000679.1:g.80685255T>G	GRCh37
NC_000017.9:g.78278544T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*208T>G MANE Select	ENSP00000269373.6:n.*208T>G
ENST00000269373.10:c.*208T>G	ENSP00000269373.6:n.*208T>G
ENST00000571594.1:c.53+212T>G	ENSP00000459751.1:n.53+212T>G
ENST00000574832.5:c.*1095T>G	ENSP00000460869.1:n.*1095T>G
NM_024619.3:c.*208T>G	NP_078895.2:n.*208T>G
NR_046408.1:n.1316T>G
XM_024450948.1:c.*208T>G	XP_024306716.1:n.*208T>G
NM_024619.4:c.*208T>G MANE Select	NP_078895.2:n.*208T>G
NR_046408.2:n.1316T>G