Canonical Allele Identifier: CA2466844444

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954284_154954285delinsGT , CM000685.2:g.154954284_154954285delinsGT	GRCh38
NC_000023.10:g.154182559_154182560delinsGT , CM000685.1:g.154182559_154182560delinsGT	GRCh37
NC_000023.9:g.153835753_153835754delinsGT	NCBI36
NG_011403.1:g.73439_73440delinsAC
NG_011403.2:g.73439_73440delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1753-243_1753-242delinsAC MANE Select	ENSP00000353393.4:n.1753-243_1753-242delinsAC
ENST00000647125.1:c.*1629-243_*1629-242delinsAC	ENSP00000496062.1:n.*1629-243_*1629-242delinsAC
ENST00000360256.8:c.1753-243_1753-242delinsAC	ENSP00000353393.4:n.1753-243_1753-242delinsAC
NM_000132.3:c.1753-243_1753-242delinsAC	NP_000123.1:n.1753-243_1753-242delinsAC
XM_011531126.1:c.1648-243_1648-242delinsAC	XP_011529428.1:n.1648-243_1648-242delinsAC
NM_000132.4:c.1753-243_1753-242delinsAC MANE Select	NP_000123.1:n.1753-243_1753-242delinsAC