Canonical Allele Identifier: CA2695168193

Gene: F8

Linked Data

• gnomAD v4: X-154905085-T-TAG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905085_154905086insAG , CM000685.2:g.154905085_154905086insAG	GRCh38
NC_000023.10:g.154133360_154133361insAG , CM000685.1:g.154133360_154133361insAG	GRCh37
NC_000023.9:g.153786554_153786555insAG	NCBI36
NG_011403.1:g.122638_122639insCT
NG_011403.2:g.122638_122639insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-63_5374-62insCT MANE Select	ENSP00000353393.4:n.5374-63_5374-62insCT
ENST00000360256.8:c.5374-63_5374-62insCT	ENSP00000353393.4:n.5374-63_5374-62insCT
NM_000132.3:c.5374-63_5374-62insCT	NP_000123.1:n.5374-63_5374-62insCT
XM_011531126.1:c.5269-63_5269-62insCT	XP_011529428.1:n.5269-63_5269-62insCT
NM_000132.4:c.5374-63_5374-62insCT MANE Select	NP_000123.1:n.5374-63_5374-62insCT