Canonical Allele Identifier: CA2695168156

Gene: F8

Linked Data

• gnomAD v4: X-154905039-G-GAA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905040_154905041insAA , CM000685.2:g.154905040_154905041insAA	GRCh38
NC_000023.10:g.154133315_154133316insAA , CM000685.1:g.154133315_154133316insAA	GRCh37
NC_000023.9:g.153786509_153786510insAA	NCBI36
NG_011403.1:g.122684_122685insTT
NG_011403.2:g.122684_122685insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-17_5374-16insTT MANE Select	ENSP00000353393.4:n.5374-17_5374-16insTT
ENST00000360256.8:c.5374-17_5374-16insTT	ENSP00000353393.4:n.5374-17_5374-16insTT
NM_000132.3:c.5374-17_5374-16insTT	NP_000123.1:n.5374-17_5374-16insTT
XM_011531126.1:c.5269-17_5269-16insTT	XP_011529428.1:n.5269-17_5269-16insTT
NM_000132.4:c.5374-17_5374-16insTT MANE Select	NP_000123.1:n.5374-17_5374-16insTT