Canonical Allele Identifier: CA2466844439

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154954274_154954290delinsACTGAACTTAGTTTTTT , CM000685.2:g.154954274_154954290delinsACTGAACTTAGTTTTTT	GRCh38
NC_000023.10:g.154182549_154182565delinsACTGAACTTAGTTTTTT , CM000685.1:g.154182549_154182565delinsACTGAACTTAGTTTTTT	GRCh37
NC_000023.9:g.153835743_153835759delinsACTGAACTTAGTTTTTT	NCBI36
NG_011403.1:g.73434_73450delinsAAAAAACTAAGTTCAGT
NG_011403.2:g.73434_73450delinsAAAAAACTAAGTTCAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1753-248_1753-232delinsAAAAAACTAAGTTCAGT MANE Select	ENSP00000353393.4:n.1753-248_1753-232delinsAAAAAACTAAGTTCAGT
ENST00000647125.1:c.*1629-248_*1629-232delinsAAAAAACTAAGTTCAGT	ENSP00000496062.1:n.*1629-248_*1629-232delinsAAAAAACTAAGTTCAG...
ENST00000360256.8:c.1753-248_1753-232delinsAAAAAACTAAGTTCAGT	ENSP00000353393.4:n.1753-248_1753-232delinsAAAAAACTAAGTTCAGT
NM_000132.3:c.1753-248_1753-232delinsAAAAAACTAAGTTCAGT	NP_000123.1:n.1753-248_1753-232delinsAAAAAACTAAGTTCAGT
XM_011531126.1:c.1648-248_1648-232delinsAAAAAACTAAGTTCAGT	XP_011529428.1:n.1648-248_1648-232delinsAAAAAACTAAGTTCAGT
NM_000132.4:c.1753-248_1753-232delinsAAAAAACTAAGTTCAGT MANE Select	NP_000123.1:n.1753-248_1753-232delinsAAAAAACTAAGTTCAGT