Canonical Allele Identifier: CA775764238

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1487614120
• gnomAD v3: 17-82727501-A-G
• gnomAD v4: 17-82727501-A-G
• MyVariant Identifiers: chr17:g.80685377A>G (hg19) ; chr17:g.82727501A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727501A>G , CM000679.2:g.82727501A>G	GRCh38
NC_000017.10:g.80685377A>G , CM000679.1:g.80685377A>G	GRCh37
NC_000017.9:g.78278666A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*330A>G MANE Select	ENSP00000269373.6:n.*330A>G
ENST00000269373.10:c.*330A>G	ENSP00000269373.6:n.*330A>G
ENST00000571594.1:c.53+334A>G	ENSP00000459751.1:n.53+334A>G
ENST00000574832.5:c.*1217A>G	ENSP00000460869.1:n.*1217A>G
NM_024619.3:c.*330A>G	NP_078895.2:n.*330A>G
NR_046408.1:n.1438A>G
XM_024450948.1:c.*330A>G	XP_024306716.1:n.*330A>G
NM_024619.4:c.*330A>G MANE Select	NP_078895.2:n.*330A>G
NR_046408.2:n.1438A>G