Canonical Allele Identifier: CA1008977058
Gene: F5 HGNC NCBI

Linked Data

gnomAD v3: 1-169549616-T-TA
gnomAD v4: 1-169549616-T-TA
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169549616_169549617insA , CM000663.2:g.169549616_169549617insA GRCh38
NC_000001.10:g.169518854_169518855insA , CM000663.1:g.169518854_169518855insA GRCh37
NC_000001.9:g.167785478_167785479insA NCBI36
NG_011806.1:g.41915_41916insT , LRG_553:g.41915_41916insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1611+184_1611+185insT MANE Select ENSP00000356771.3:n.1611+184_1611+185insT
ENST00000367796.3:c.1611+184_1611+185insT ENSP00000356770.3:n.1611+184_1611+185insT
ENST00000367797.7:c.1611+184_1611+185insT ENSP00000356771.3:n.1611+184_1611+185insT
NM_000130.4:c.1611+184_1611+185insT , LRG_553t1:c.1611+184_1611+185insT NP_000121.2:n.1611+184_1611+185insT
XM_017000660.2:c.1200+184_1200+185insT XP_016856149.1:n.1200+184_1200+185insT
NM_000130.5:c.1611+184_1611+185insT MANE Select NP_000121.2:n.1611+184_1611+185insT
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