Canonical Allele Identifier: CA775764497

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1410652736
• gnomAD v3: 17-82727963-TAATA-T
• gnomAD v4: 17-82727963-TAATA-T
• MyVariant Identifiers: chr17:g.80685840_80685843del (hg19) ; chr17:g.82727964_82727967del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727967_82727970del , CM000679.2:g.82727967_82727970del	GRCh38
NC_000017.10:g.80685843_80685846del , CM000679.1:g.80685843_80685846del	GRCh37
NC_000017.9:g.78279132_78279135del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*796_*799del MANE Select	ENSP00000269373.6:n.*796_*799del
ENST00000269373.10:c.*796_*799del	ENSP00000269373.6:n.*796_*799del
ENST00000571594.1:c.53+800_53+803del	ENSP00000459751.1:n.53+800_53+803del
NM_024619.3:c.*796_*799del	NP_078895.2:n.*796_*799del
NR_046408.1:n.1904_1907del
XM_024450948.1:c.*796_*799del	XP_024306716.1:n.*796_*799del
NM_024619.4:c.*796_*799del MANE Select	NP_078895.2:n.*796_*799del
NR_046408.2:n.1904_1907del