Canonical Allele Identifier: CA645251978
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154133314delinsAG (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154905038_154905039insA , CM000685.2:g.154905038_154905039insA GRCh38
NC_000023.10:g.154133313_154133314insA , CM000685.1:g.154133313_154133314insA GRCh37
NC_000023.9:g.153786507_153786508insA NCBI36
NG_011403.1:g.122685_122686insT
NG_011403.2:g.122685_122686insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5374-16_5374-15insT MANE Select ENSP00000353393.4:n.5374-16_5374-15insT
ENST00000360256.8:c.5374-16_5374-15insT ENSP00000353393.4:n.5374-16_5374-15insT
NM_000132.3:c.5374-16_5374-15insT NP_000123.1:n.5374-16_5374-15insT
XM_011531126.1:c.5269-16_5269-15insT XP_011529428.1:n.5269-16_5269-15insT
NM_000132.4:c.5374-16_5374-15insT MANE Select NP_000123.1:n.5374-16_5374-15insT