Canonical Allele Identifier: CA2466828497

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154905041_154905044delinsCAAA , CM000685.2:g.154905041_154905044delinsCAAA	GRCh38
NC_000023.10:g.154133316_154133319delinsCAAA , CM000685.1:g.154133316_154133319delinsCAAA	GRCh37
NC_000023.9:g.153786510_153786513delinsCAAA	NCBI36
NG_011403.1:g.122680_122683delinsTTTG
NG_011403.2:g.122680_122683delinsTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5374-21_5374-18delinsTTTG MANE Select	ENSP00000353393.4:n.5374-21_5374-18delinsTTTG
ENST00000360256.8:c.5374-21_5374-18delinsTTTG	ENSP00000353393.4:n.5374-21_5374-18delinsTTTG
NM_000132.3:c.5374-21_5374-18delinsTTTG	NP_000123.1:n.5374-21_5374-18delinsTTTG
XM_011531126.1:c.5269-21_5269-18delinsTTTG	XP_011529428.1:n.5269-21_5269-18delinsTTTG
NM_000132.4:c.5374-21_5374-18delinsTTTG MANE Select	NP_000123.1:n.5374-21_5374-18delinsTTTG