Canonical Allele Identifier: CA2466845385

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957183_154957184delinsCA , CM000685.2:g.154957183_154957184delinsCA	GRCh38
NC_000023.10:g.154185458_154185459delinsCA , CM000685.1:g.154185458_154185459delinsCA	GRCh37
NC_000023.9:g.153838652_153838653delinsCA	NCBI36
NG_011403.1:g.70540_70541delinsTG
NG_011403.2:g.70540_70541delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1538-13_1538-12delinsTG MANE Select	ENSP00000353393.4:n.1538-13_1538-12delinsTG
ENST00000647125.1:c.*1414-13_*1414-12delinsTG	ENSP00000496062.1:n.*1414-13_*1414-12delinsTG
ENST00000360256.8:c.1538-13_1538-12delinsTG	ENSP00000353393.4:n.1538-13_1538-12delinsTG
NM_000132.3:c.1538-13_1538-12delinsTG	NP_000123.1:n.1538-13_1538-12delinsTG
XM_011531126.1:c.1433-13_1433-12delinsTG	XP_011529428.1:n.1433-13_1433-12delinsTG
NM_000132.4:c.1538-13_1538-12delinsTG MANE Select	NP_000123.1:n.1538-13_1538-12delinsTG