Canonical Allele Identifier: CA2279174176

Gene: FN3KRP

Linked Data

• dbSNP Id: rs2046850561

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727937A>T , CM000679.2:g.82727937A>T	GRCh38
NC_000017.10:g.80685813A>T , CM000679.1:g.80685813A>T	GRCh37
NC_000017.9:g.78279102A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*766A>T MANE Select	ENSP00000269373.6:n.*766A>T
ENST00000269373.10:c.*766A>T	ENSP00000269373.6:n.*766A>T
ENST00000571594.1:c.53+770A>T	ENSP00000459751.1:n.53+770A>T
NM_024619.3:c.*766A>T	NP_078895.2:n.*766A>T
NR_046408.1:n.1874A>T
XM_024450948.1:c.*766A>T	XP_024306716.1:n.*766A>T
NM_024619.4:c.*766A>T MANE Select	NP_078895.2:n.*766A>T
NR_046408.2:n.1874A>T