Canonical Allele Identifier: CA873361072

Gene: F8

Linked Data

• dbSNP Id: rs1292729232
• MyVariant Identifiers: chrX:g.154837746del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837746del , CM000685.2:g.154837746del	GRCh38
NC_000023.10:g.154066021del , CM000685.1:g.154066021del	GRCh37
NC_000023.9:g.153719215del	NCBI36
NG_011403.1:g.189978del
NG_033065.1:g.1917del
NG_011403.2:g.189978del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6907del MANE Select	ENSP00000353393.4:p.Gln2303ArgfsTer11
ENST00000644698.1:c.640del	ENSP00000495706.1:p.Gln214ArgfsTer11
ENST00000330287.10:c.502del	ENSP00000327895.6:p.Gln168ArgfsTer11
ENST00000360256.8:c.6907del	ENSP00000353393.4:p.Gln2303ArgfsTer11
NM_000132.3:c.6907del	NP_000123.1:p.Gln2303ArgfsTer11
NM_019863.2:c.502del	NP_063916.1:p.Gln168ArgfsTer11
XM_011531126.1:c.6802del	XP_011529428.1:p.Gln2268ArgfsTer11
NM_000132.4:c.6907del MANE Select	NP_000123.1:p.Gln2303ArgfsTer11
NM_019863.3:c.502del	NP_063916.1:p.Gln168ArgfsTer11