Canonical Allele Identifier: CA2810673889

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727611T>C , CM000679.2:g.82727611T>C	GRCh38
NC_000017.10:g.80685487T>C , CM000679.1:g.80685487T>C	GRCh37
NC_000017.9:g.78278776T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*440T>C MANE Select	ENSP00000269373.6:n.*440T>C
ENST00000269373.10:c.*440T>C	ENSP00000269373.6:n.*440T>C
ENST00000571594.1:c.53+444T>C	ENSP00000459751.1:n.53+444T>C
NM_024619.3:c.*440T>C	NP_078895.2:n.*440T>C
NR_046408.1:n.1548T>C
XM_024450948.1:c.*440T>C	XP_024306716.1:n.*440T>C
NM_024619.4:c.*440T>C MANE Select	NP_078895.2:n.*440T>C
NR_046408.2:n.1548T>C