Canonical Allele Identifier: CA2640699565

Gene: FN3KRP

Linked Data

• gnomAD v4: 17-82727251-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727251G>C , CM000679.2:g.82727251G>C	GRCh38
NC_000017.10:g.80685127G>C , CM000679.1:g.80685127G>C	GRCh37
NC_000017.9:g.78278416G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*80G>C MANE Select	ENSP00000269373.6:n.*80G>C
ENST00000269373.10:c.*80G>C	ENSP00000269373.6:n.*80G>C
ENST00000571594.1:c.53+84G>C	ENSP00000459751.1:n.53+84G>C
ENST00000574832.5:c.*967G>C	ENSP00000460869.1:n.*967G>C
NM_024619.3:c.*80G>C	NP_078895.2:n.*80G>C
NR_046408.1:n.1188G>C
XM_024450948.1:c.*80G>C	XP_024306716.1:n.*80G>C
NM_024619.4:c.*80G>C MANE Select	NP_078895.2:n.*80G>C
NR_046408.2:n.1188G>C