Canonical Allele Identifier: CA502803113

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046845148
• gnomAD v3: 17-82727227-C-T
• gnomAD v4: 17-82727227-C-T
• MyVariant Identifiers: chr17:g.80685103C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727227C>T , CM000679.2:g.82727227C>T	GRCh38
NC_000017.10:g.80685103C>T , CM000679.1:g.80685103C>T	GRCh37
NC_000017.9:g.78278392C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*56C>T MANE Select	ENSP00000269373.6:n.*56C>T
ENST00000269373.10:c.*56C>T	ENSP00000269373.6:n.*56C>T
ENST00000571594.1:c.53+60C>T	ENSP00000459751.1:n.53+60C>T
ENST00000574832.5:c.*943C>T	ENSP00000460869.1:n.*943C>T
NM_024619.3:c.*56C>T	NP_078895.2:n.*56C>T
NR_046408.1:n.1164C>T
XM_024450948.1:c.*56C>T	XP_024306716.1:n.*56C>T
NM_024619.4:c.*56C>T MANE Select	NP_078895.2:n.*56C>T
NR_046408.2:n.1164C>T