Canonical Allele Identifier: CA890929700
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1252350704
MyVariant Identifiers: chr1:g.169524261_169524262insG (hg19) chr1:g.169555023_169555024insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555028dup , CM000663.2:g.169555028dup GRCh38
NC_000001.10:g.169524266dup , CM000663.1:g.169524266dup GRCh37
NC_000001.9:g.167790890dup NCBI36
NG_011806.1:g.36508dup , LRG_553:g.36508dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1118+158dup MANE Select ENSP00000356771.3:n.1118+158dup
ENST00000367796.3:c.1118+158dup ENSP00000356770.3:n.1118+158dup
ENST00000367797.7:c.1118+158dup ENSP00000356771.3:n.1118+158dup
NM_000130.4:c.1118+158dup , LRG_553t1:c.1118+158dup NP_000121.2:n.1118+158dup
XM_017000660.2:c.707+158dup XP_016856149.1:n.707+158dup
NM_000130.5:c.1118+158dup MANE Select NP_000121.2:n.1118+158dup
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