Canonical Allele Identifier: CA2640697498

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727484-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727484G>T , CM000679.2:g.82727484G>T	GRCh38
NC_000017.10:g.80685360G>T , CM000679.1:g.80685360G>T	GRCh37
NC_000017.9:g.78278649G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*313G>T MANE Select	ENSP00000269373.6:n.*313G>T
ENST00000269373.10:c.*313G>T	ENSP00000269373.6:n.*313G>T
ENST00000571594.1:c.53+317G>T	ENSP00000459751.1:n.53+317G>T
ENST00000574832.5:c.*1200G>T	ENSP00000460869.1:n.*1200G>T
NM_024619.3:c.*313G>T	NP_078895.2:n.*313G>T
NR_046408.1:n.1421G>T
XM_024450948.1:c.*313G>T	XP_024306716.1:n.*313G>T
NM_024619.4:c.*313G>T MANE Select	NP_078895.2:n.*313G>T
NR_046408.2:n.1421G>T