Canonical Allele Identifier: CA658546465

Gene: F8

Linked Data

• COSMIC: COSN20082305

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957182_154957183insA , CM000685.2:g.154957182_154957183insA	GRCh38
NC_000023.10:g.154185457_154185458insA , CM000685.1:g.154185457_154185458insA	GRCh37
NC_000023.9:g.153838651_153838652insA	NCBI36
NG_011403.1:g.70541_70542insT
NG_011403.2:g.70541_70542insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-12_1538-11insT MANE Select	ENSP00000353393.4:n.1538-12_1538-11insT
ENST00000647125.1:c.*1414-12_*1414-11insT	ENSP00000496062.1:n.*1414-12_*1414-11insT
ENST00000360256.8:c.1538-12_1538-11insT	ENSP00000353393.4:n.1538-12_1538-11insT
NM_000132.3:c.1538-12_1538-11insT	NP_000123.1:n.1538-12_1538-11insT
XM_011531126.1:c.1433-12_1433-11insT	XP_011529428.1:n.1433-12_1433-11insT
NM_000132.4:c.1538-12_1538-11insT MANE Select	NP_000123.1:n.1538-12_1538-11insT