Canonical Allele Identifier: CA2279173826

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727219C= , CM000679.2:g.82727219C=	GRCh38
NC_000017.10:g.80685095C= , CM000679.1:g.80685095C=	GRCh37
NC_000017.9:g.78278384C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*48C= MANE Select	ENSP00000269373.6:n.*48C=
ENST00000269373.10:c.*48C=	ENSP00000269373.6:n.*48C=
ENST00000571594.1:c.53+52C=	ENSP00000459751.1:n.53+52C=
ENST00000574832.5:c.*935C=	ENSP00000460869.1:n.*935C=
NM_024619.3:c.*48C=	NP_078895.2:n.*48C=
NR_046408.1:n.1156C=
XM_024450948.1:c.*48C=	XP_024306716.1:n.*48C=
NM_024619.4:c.*48C= MANE Select	NP_078895.2:n.*48C=
NR_046408.2:n.1156C=