Canonical Allele Identifier: CA2466814968

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860421_154860422delinsGA , CM000685.2:g.154860421_154860422delinsGA	GRCh38
NC_000023.10:g.154088696_154088697delinsGA , CM000685.1:g.154088696_154088697delinsGA	GRCh37
NC_000023.9:g.153741890_153741891delinsGA	NCBI36
NG_011403.1:g.167302_167303delinsTC
NG_011403.2:g.167302_167303delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+10_6900+11delinsTC MANE Select	ENSP00000353393.4:n.6900+10_6900+11delinsTC
ENST00000644698.1:c.633+10_633+11delinsTC	ENSP00000495706.1:n.633+10_633+11delinsTC
ENST00000330287.10:c.495+10_495+11delinsTC	ENSP00000327895.6:n.495+10_495+11delinsTC
ENST00000360256.8:c.6900+10_6900+11delinsTC	ENSP00000353393.4:n.6900+10_6900+11delinsTC
NM_000132.3:c.6900+10_6900+11delinsTC	NP_000123.1:n.6900+10_6900+11delinsTC
NM_019863.2:c.495+10_495+11delinsTC	NP_063916.1:n.495+10_495+11delinsTC
XM_011531126.1:c.6795+10_6795+11delinsTC	XP_011529428.1:n.6795+10_6795+11delinsTC
NM_000132.4:c.6900+10_6900+11delinsTC MANE Select	NP_000123.1:n.6900+10_6900+11delinsTC
NM_019863.3:c.495+10_495+11delinsTC	NP_063916.1:n.495+10_495+11delinsTC