Canonical Allele Identifier: CA401621861

Gene: FN3K

Linked Data

• MyVariant Identifiers: chr17:g.80708509G>T (hg19) ; chr17:g.82750633G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82750633G>T , CM000679.2:g.82750633G>T	GRCh38
NC_000017.10:g.80708509G>T , CM000679.1:g.80708509G>T	GRCh37
NC_000017.9:g.78301798G>T	NCBI36
NG_011721.1:g.3570G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000300784.8:c.808G>T MANE Select	ENSP00000300784.7:p.Ala270Ser
ENST00000300784.7:c.808G>T	ENSP00000300784.7:p.Ala270Ser
NM_022158.3:c.808G>T	NP_071441.1:p.Ala270Ser
XM_024450872.1:c.658G>T	XP_024306640.1:p.Ala220Ser
NM_022158.4:c.808G>T MANE Select	NP_071441.1:p.Ala270Ser