Canonical Allele Identifier: CA295269621

Gene: FN3KRP

Linked Data

• dbSNP Id: rs537853921
• gnomAD v3: 17-82727449-G-T
• gnomAD v4: 17-82727449-G-T
• MyVariant Identifiers: chr17:g.80685325G>T (hg19) ; chr17:g.82727449G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727449G>T , CM000679.2:g.82727449G>T	GRCh38
NC_000017.10:g.80685325G>T , CM000679.1:g.80685325G>T	GRCh37
NC_000017.9:g.78278614G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*278G>T MANE Select	ENSP00000269373.6:n.*278G>T
ENST00000269373.10:c.*278G>T	ENSP00000269373.6:n.*278G>T
ENST00000571594.1:c.53+282G>T	ENSP00000459751.1:n.53+282G>T
ENST00000574832.5:c.*1165G>T	ENSP00000460869.1:n.*1165G>T
NM_024619.3:c.*278G>T	NP_078895.2:n.*278G>T
NR_046408.1:n.1386G>T
XM_024450948.1:c.*278G>T	XP_024306716.1:n.*278G>T
NM_024619.4:c.*278G>T MANE Select	NP_078895.2:n.*278G>T
NR_046408.2:n.1386G>T