Canonical Allele Identifier: CA2695168199

Gene: F8

Linked Data

• gnomAD v4: X-154905090-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905090_154905091insA , CM000685.2:g.154905090_154905091insA	GRCh38
NC_000023.10:g.154133365_154133366insA , CM000685.1:g.154133365_154133366insA	GRCh37
NC_000023.9:g.153786559_153786560insA	NCBI36
NG_011403.1:g.122633_122634insT
NG_011403.2:g.122633_122634insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-68_5374-67insT MANE Select	ENSP00000353393.4:n.5374-68_5374-67insT
ENST00000360256.8:c.5374-68_5374-67insT	ENSP00000353393.4:n.5374-68_5374-67insT
NM_000132.3:c.5374-68_5374-67insT	NP_000123.1:n.5374-68_5374-67insT
XM_011531126.1:c.5269-68_5269-67insT	XP_011529428.1:n.5269-68_5269-67insT
NM_000132.4:c.5374-68_5374-67insT MANE Select	NP_000123.1:n.5374-68_5374-67insT