Canonical Allele Identifier: CA2695237898
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928646_154928648del , CM000685.2:g.154928646_154928648del GRCh38
NC_000023.10:g.154156921_154156923del , CM000685.1:g.154156921_154156923del GRCh37
NC_000023.9:g.153810115_153810117del NCBI36
NG_011403.1:g.99078_99080del
NG_011403.2:g.99078_99080del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5144_5146del MANE Select ENSP00000353393.4:p.Arg1715del
ENST00000360256.8:c.5144_5146del ENSP00000353393.4:p.Arg1715del
NM_000132.3:c.5144_5146del NP_000123.1:p.Arg1715del
XM_011531126.1:c.5039_5041del XP_011529428.1:p.Arg1680del
NM_000132.4:c.5144_5146del MANE Select NP_000123.1:p.Arg1715del
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