Canonical Allele Identifier: CA2279173936

Gene: FN3KRP

Linked Data

• dbSNP Id: rs1598336802
• gnomAD v4: 17-82727466-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727466A>C , CM000679.2:g.82727466A>C	GRCh38
NC_000017.10:g.80685342A>C , CM000679.1:g.80685342A>C	GRCh37
NC_000017.9:g.78278631A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000269373.11:c.*295A>C MANE Select	ENSP00000269373.6:n.*295A>C
ENST00000269373.10:c.*295A>C	ENSP00000269373.6:n.*295A>C
ENST00000571594.1:c.53+299A>C	ENSP00000459751.1:n.53+299A>C
ENST00000574832.5:c.*1182A>C	ENSP00000460869.1:n.*1182A>C
NM_024619.3:c.*295A>C	NP_078895.2:n.*295A>C
NR_046408.1:n.1403A>C
XM_024450948.1:c.*295A>C	XP_024306716.1:n.*295A>C
NM_024619.4:c.*295A>C MANE Select	NP_078895.2:n.*295A>C
NR_046408.2:n.1403A>C