Canonical Allele Identifier: CA775764459

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1351792203
• gnomAD v3: 17-82727936-GAC-G
• gnomAD v4: 17-82727936-GAC-G
• MyVariant Identifiers: chr17:g.80685813_80685814del (hg19) ; chr17:g.82727937_82727938del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727938_82727939del , CM000679.2:g.82727938_82727939del	GRCh38
NC_000017.10:g.80685814_80685815del , CM000679.1:g.80685814_80685815del	GRCh37
NC_000017.9:g.78279103_78279104del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*767_*768del MANE Select	ENSP00000269373.6:n.*767_*768del
ENST00000269373.10:c.*767_*768del	ENSP00000269373.6:n.*767_*768del
ENST00000571594.1:c.53+771_53+772del	ENSP00000459751.1:n.53+771_53+772del
NM_024619.3:c.*767_*768del	NP_078895.2:n.*767_*768del
NR_046408.1:n.1875_1876del
XM_024450948.1:c.*767_*768del	XP_024306716.1:n.*767_*768del
NM_024619.4:c.*767_*768del MANE Select	NP_078895.2:n.*767_*768del
NR_046408.2:n.1875_1876del