Canonical Allele Identifier: CA2640697421

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727452-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727452G>T , CM000679.2:g.82727452G>T	GRCh38
NC_000017.10:g.80685328G>T , CM000679.1:g.80685328G>T	GRCh37
NC_000017.9:g.78278617G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*281G>T MANE Select	ENSP00000269373.6:n.*281G>T
ENST00000269373.10:c.*281G>T	ENSP00000269373.6:n.*281G>T
ENST00000571594.1:c.53+285G>T	ENSP00000459751.1:n.53+285G>T
ENST00000574832.5:c.*1168G>T	ENSP00000460869.1:n.*1168G>T
NM_024619.3:c.*281G>T	NP_078895.2:n.*281G>T
NR_046408.1:n.1389G>T
XM_024450948.1:c.*281G>T	XP_024306716.1:n.*281G>T
NM_024619.4:c.*281G>T MANE Select	NP_078895.2:n.*281G>T
NR_046408.2:n.1389G>T