Canonical Allele Identifier: CA2695237117

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837751del , CM000685.2:g.154837751del	GRCh38
NC_000023.10:g.154066026del , CM000685.1:g.154066026del	GRCh37
NC_000023.9:g.153719220del	NCBI36
NG_011403.1:g.189977del
NG_033065.1:g.1916del
NG_011403.2:g.189977del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6906del MANE Select	ENSP00000353393.4:p.Gln2303ArgfsTer11
ENST00000644698.1:c.639del	ENSP00000495706.1:p.Gln214ArgfsTer11
ENST00000330287.10:c.501del	ENSP00000327895.6:p.Gln168ArgfsTer11
ENST00000360256.8:c.6906del	ENSP00000353393.4:p.Gln2303ArgfsTer11
NM_000132.3:c.6906del	NP_000123.1:p.Gln2303ArgfsTer11
NM_019863.2:c.501del	NP_063916.1:p.Gln168ArgfsTer11
XM_011531126.1:c.6801del	XP_011529428.1:p.Gln2268ArgfsTer11
NM_000132.4:c.6906del MANE Select	NP_000123.1:p.Gln2303ArgfsTer11
NM_019863.3:c.501del	NP_063916.1:p.Gln168ArgfsTer11