Canonical Allele Identifier: CA2649036286
Gene: F5 HGNC NCBI

Linked Data

gnomAD v4: 1-169555153-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555156del , CM000663.2:g.169555156del GRCh38
NC_000001.10:g.169524394del , CM000663.1:g.169524394del GRCh37
NC_000001.9:g.167791018del NCBI36
NG_011806.1:g.36378del , LRG_553:g.36378del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1118+28del MANE Select ENSP00000356771.3:n.1118+28del
ENST00000367796.3:c.1118+28del ENSP00000356770.3:n.1118+28del
ENST00000367797.7:c.1118+28del ENSP00000356771.3:n.1118+28del
NM_000130.4:c.1118+28del , LRG_553t1:c.1118+28del NP_000121.2:n.1118+28del
XM_017000660.2:c.707+28del XP_016856149.1:n.707+28del
NM_000130.5:c.1118+28del MANE Select NP_000121.2:n.1118+28del
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