Canonical Allele Identifier: CA890928379
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1338977637
MyVariant Identifiers: chr1:g.169521463del (hg19) chr1:g.169552225del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552225del , CM000663.2:g.169552225del GRCh38
NC_000001.10:g.169521463del , CM000663.1:g.169521463del GRCh37
NC_000001.9:g.167788087del NCBI36
NG_011806.1:g.39307del , LRG_553:g.39307del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1296+332del MANE Select ENSP00000356771.3:n.1296+332del
ENST00000367796.3:c.1296+332del ENSP00000356770.3:n.1296+332del
ENST00000367797.7:c.1296+332del ENSP00000356771.3:n.1296+332del
NM_000130.4:c.1296+332del , LRG_553t1:c.1296+332del NP_000121.2:n.1296+332del
XM_017000660.2:c.885+332del XP_016856149.1:n.885+332del
NM_000130.5:c.1296+332del MANE Select NP_000121.2:n.1296+332del
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