Canonical Allele Identifier: CA2579752263
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863112_154863113del , CM000685.2:g.154863112_154863113del GRCh38
NC_000023.10:g.154091387_154091388del , CM000685.1:g.154091387_154091388del GRCh37
NC_000023.9:g.153744581_153744582del NCBI36
NG_011403.1:g.164612_164613del
NG_011403.2:g.164612_164613del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6545_6546del MANE Select ENSP00000353393.4:p.Arg2182HisfsTer7
ENST00000644698.1:c.278_279del ENSP00000495706.1:p.Arg93HisfsTer7
ENST00000330287.10:c.140_141del ENSP00000327895.6:p.Arg47HisfsTer7
ENST00000360256.8:c.6545_6546del ENSP00000353393.4:p.Arg2182HisfsTer7
NM_000132.3:c.6545_6546del NP_000123.1:p.Arg2182HisfsTer7
NM_019863.2:c.140_141del NP_063916.1:p.Arg47HisfsTer7
XM_011531126.1:c.6440_6441del XP_011529428.1:p.Arg2147HisfsTer7
NM_000132.4:c.6545_6546del MANE Select NP_000123.1:p.Arg2182HisfsTer7
NM_019863.3:c.140_141del NP_063916.1:p.Arg47HisfsTer7