Canonical Allele Identifier: CA2579752218

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860397_154860405del , CM000685.2:g.154860397_154860405del	GRCh38
NC_000023.10:g.154088672_154088680del , CM000685.1:g.154088672_154088680del	GRCh37
NC_000023.9:g.153741866_153741874del	NCBI36
NG_011403.1:g.167322_167330del
NG_011403.2:g.167322_167330del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+30_6900+38del MANE Select	ENSP00000353393.4:n.6900+30_6900+38del
ENST00000644698.1:c.633+30_633+38del	ENSP00000495706.1:n.633+30_633+38del
ENST00000330287.10:c.495+30_495+38del	ENSP00000327895.6:n.495+30_495+38del
ENST00000360256.8:c.6900+30_6900+38del	ENSP00000353393.4:n.6900+30_6900+38del
NM_000132.3:c.6900+30_6900+38del	NP_000123.1:n.6900+30_6900+38del
NM_019863.2:c.495+30_495+38del	NP_063916.1:n.495+30_495+38del
XM_011531126.1:c.6795+30_6795+38del	XP_011529428.1:n.6795+30_6795+38del
NM_000132.4:c.6900+30_6900+38del MANE Select	NP_000123.1:n.6900+30_6900+38del
NM_019863.3:c.495+30_495+38del	NP_063916.1:n.495+30_495+38del