Canonical Allele Identifier: CA2695237122

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860446del , CM000685.2:g.154860446del	GRCh38
NC_000023.10:g.154088721del , CM000685.1:g.154088721del	GRCh37
NC_000023.9:g.153741915del	NCBI36
NG_011403.1:g.167279del
NG_011403.2:g.167279del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.6887del MANE Select	ENSP00000353393.4:p.Asn2296MetfsTer4
ENST00000644698.1:c.620del	ENSP00000495706.1:p.Asn207MetfsTer4
ENST00000330287.10:c.482del	ENSP00000327895.6:p.Asn161MetfsTer4
ENST00000360256.8:c.6887del	ENSP00000353393.4:p.Asn2296MetfsTer4
NM_000132.3:c.6887del	NP_000123.1:p.Asn2296MetfsTer4
NM_019863.2:c.482del	NP_063916.1:p.Asn161MetfsTer4
XM_011531126.1:c.6782del	XP_011529428.1:p.Asn2261MetfsTer4
NM_000132.4:c.6887del MANE Select	NP_000123.1:p.Asn2296MetfsTer4
NM_019863.3:c.482del	NP_063916.1:p.Asn161MetfsTer4