Canonical Allele Identifier: CA2640697272

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727371-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727371A>T , CM000679.2:g.82727371A>T	GRCh38
NC_000017.10:g.80685247A>T , CM000679.1:g.80685247A>T	GRCh37
NC_000017.9:g.78278536A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*200A>T MANE Select	ENSP00000269373.6:n.*200A>T
ENST00000269373.10:c.*200A>T	ENSP00000269373.6:n.*200A>T
ENST00000571594.1:c.53+204A>T	ENSP00000459751.1:n.53+204A>T
ENST00000574832.5:c.*1087A>T	ENSP00000460869.1:n.*1087A>T
NM_024619.3:c.*200A>T	NP_078895.2:n.*200A>T
NR_046408.1:n.1308A>T
XM_024450948.1:c.*200A>T	XP_024306716.1:n.*200A>T
NM_024619.4:c.*200A>T MANE Select	NP_078895.2:n.*200A>T
NR_046408.2:n.1308A>T