Canonical Allele Identifier: CA2640697393

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727438-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727439del , CM000679.2:g.82727439del	GRCh38
NC_000017.10:g.80685315del , CM000679.1:g.80685315del	GRCh37
NC_000017.9:g.78278604del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*268del MANE Select	ENSP00000269373.6:n.*268del
ENST00000269373.10:c.*268del	ENSP00000269373.6:n.*268del
ENST00000571594.1:c.53+272del	ENSP00000459751.1:n.53+272del
ENST00000574832.5:c.*1155del	ENSP00000460869.1:n.*1155del
NM_024619.3:c.*268del	NP_078895.2:n.*268del
NR_046408.1:n.1376del
XM_024450948.1:c.*268del	XP_024306716.1:n.*268del
NM_024619.4:c.*268del MANE Select	NP_078895.2:n.*268del
NR_046408.2:n.1376del