Canonical Allele Identifier: CA2279173917

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727431_82727433delinsTCA , CM000679.2:g.82727431_82727433delinsTCA	GRCh38
NC_000017.10:g.80685307_80685309delinsTCA , CM000679.1:g.80685307_80685309delinsTCA	GRCh37
NC_000017.9:g.78278596_78278598delinsTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*260_*262delinsTCA MANE Select	ENSP00000269373.6:n.*260_*262delinsTCA
ENST00000269373.10:c.*260_*262delinsTCA	ENSP00000269373.6:n.*260_*262delinsTCA
ENST00000571594.1:c.53+264_53+266delinsTCA	ENSP00000459751.1:n.53+264_53+266delinsTCA
ENST00000574832.5:c.*1147_*1149delinsTCA	ENSP00000460869.1:n.*1147_*1149delinsTCA
NM_024619.3:c.*260_*262delinsTCA	NP_078895.2:n.*260_*262delinsTCA
NR_046408.1:n.1368_1370delinsTCA
XM_024450948.1:c.*260_*262delinsTCA	XP_024306716.1:n.*260_*262delinsTCA
NM_024619.4:c.*260_*262delinsTCA MANE Select	NP_078895.2:n.*260_*262delinsTCA
NR_046408.2:n.1368_1370delinsTCA