Canonical Allele Identifier: CA2640697353

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727424-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727424C>T , CM000679.2:g.82727424C>T	GRCh38
NC_000017.10:g.80685300C>T , CM000679.1:g.80685300C>T	GRCh37
NC_000017.9:g.78278589C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*253C>T MANE Select	ENSP00000269373.6:n.*253C>T
ENST00000269373.10:c.*253C>T	ENSP00000269373.6:n.*253C>T
ENST00000571594.1:c.53+257C>T	ENSP00000459751.1:n.53+257C>T
ENST00000574832.5:c.*1140C>T	ENSP00000460869.1:n.*1140C>T
NM_024619.3:c.*253C>T	NP_078895.2:n.*253C>T
NR_046408.1:n.1361C>T
XM_024450948.1:c.*253C>T	XP_024306716.1:n.*253C>T
NM_024619.4:c.*253C>T MANE Select	NP_078895.2:n.*253C>T
NR_046408.2:n.1361C>T