Canonical Allele Identifier: CA2695237258
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957077_154957078del , CM000685.2:g.154957077_154957078del GRCh38
NC_000023.10:g.154185352_154185353del , CM000685.1:g.154185352_154185353del GRCh37
NC_000023.9:g.153838546_153838547del NCBI36
NG_011403.1:g.70646_70647del
NG_011403.2:g.70646_70647del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1631_1632del MANE Select ENSP00000353393.4:p.Asp544AlafsTer10
ENST00000647125.1:c.*1507_*1508del ENSP00000496062.1:n.*1507_*1508del
ENST00000360256.8:c.1631_1632del ENSP00000353393.4:p.Asp544AlafsTer10
NM_000132.3:c.1631_1632del NP_000123.1:p.Asp544AlafsTer10
XM_011531126.1:c.1526_1527del XP_011529428.1:p.Asp509AlafsTer10
NM_000132.4:c.1631_1632del MANE Select NP_000123.1:p.Asp544AlafsTer10