Canonical Allele Identifier: CA295269525

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1021812470
• gnomAD v3: 17-82727295-A-G
• gnomAD v4: 17-82727295-A-G
• MyVariant Identifiers: chr17:g.80685171A>G (hg19) ; chr17:g.82727295A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727295A>G , CM000679.2:g.82727295A>G	GRCh38
NC_000017.10:g.80685171A>G , CM000679.1:g.80685171A>G	GRCh37
NC_000017.9:g.78278460A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*124A>G MANE Select	ENSP00000269373.6:n.*124A>G
ENST00000269373.10:c.*124A>G	ENSP00000269373.6:n.*124A>G
ENST00000571594.1:c.53+128A>G	ENSP00000459751.1:n.53+128A>G
ENST00000574832.5:c.*1011A>G	ENSP00000460869.1:n.*1011A>G
NM_024619.3:c.*124A>G	NP_078895.2:n.*124A>G
NR_046408.1:n.1232A>G
XM_024450948.1:c.*124A>G	XP_024306716.1:n.*124A>G
NM_024619.4:c.*124A>G MANE Select	NP_078895.2:n.*124A>G
NR_046408.2:n.1232A>G