Canonical Allele Identifier: CA2810673896

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727663A>G , CM000679.2:g.82727663A>G	GRCh38
NC_000017.10:g.80685539A>G , CM000679.1:g.80685539A>G	GRCh37
NC_000017.9:g.78278828A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000269373.11:c.*492A>G MANE Select	ENSP00000269373.6:n.*492A>G
ENST00000269373.10:c.*492A>G	ENSP00000269373.6:n.*492A>G
ENST00000571594.1:c.53+496A>G	ENSP00000459751.1:n.53+496A>G
NM_024619.3:c.*492A>G	NP_078895.2:n.*492A>G
NR_046408.1:n.1600A>G
XM_024450948.1:c.*492A>G	XP_024306716.1:n.*492A>G
NM_024619.4:c.*492A>G MANE Select	NP_078895.2:n.*492A>G
NR_046408.2:n.1600A>G