Canonical Allele Identifier: CA890938669
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1376857967
MyVariant Identifiers: chr1:g.169541824_169541825insGGAGAAATAGTTCTGG (hg19) chr1:g.169572586_169572587insGGAGAAATAGTTCTGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572587_169572602dup , CM000663.2:g.169572587_169572602dup GRCh38
NC_000001.10:g.169541825_169541840dup , CM000663.1:g.169541825_169541840dup GRCh37
NC_000001.9:g.167808449_167808464dup NCBI36
NG_011806.1:g.18930_18945dup , LRG_553:g.18930_18945dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.251-259_251-244dup MANE Select ENSP00000356771.3:n.251-259_251-244dup
ENST00000367796.3:c.251-259_251-244dup ENSP00000356770.3:n.251-259_251-244dup
ENST00000367797.7:c.251-259_251-244dup ENSP00000356771.3:n.251-259_251-244dup
NM_000130.4:c.251-259_251-244dup , LRG_553t1:c.251-259_251-244dup NP_000121.2:n.251-259_251-244dup
XM_017000660.2:c.-161-259_-161-244dup XP_016856149.1:n.-161-259_-161-244dup
NM_000130.5:c.251-259_251-244dup MANE Select NP_000121.2:n.251-259_251-244dup
Search 100 bp 5'
Search 100 bp 3'