Canonical Allele Identifier: CA519356138
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132218_154132219insA (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903943_154903944insA , CM000685.2:g.154903943_154903944insA GRCh38
NC_000023.10:g.154132218_154132219insA , CM000685.1:g.154132218_154132219insA GRCh37
NC_000023.9:g.153785412_153785413insA NCBI36
NG_011403.1:g.123780_123781insT
NG_011403.2:g.123780_123781insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5960_5961insT MANE Select ENSP00000353393.4:p.Lys1987AsnfsTer5
ENST00000360256.8:c.5960_5961insT ENSP00000353393.4:p.Lys1987AsnfsTer5
NM_000132.3:c.5960_5961insT NP_000123.1:p.Lys1987AsnfsTer5
XM_011531126.1:c.5855_5856insT XP_011529428.1:p.Lys1952AsnfsTer5
NM_000132.4:c.5960_5961insT MANE Select NP_000123.1:p.Lys1987AsnfsTer5
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