Canonical Allele Identifier: CA2695237259
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957081_154957084dup , CM000685.2:g.154957081_154957084dup GRCh38
NC_000023.10:g.154185356_154185359dup , CM000685.1:g.154185356_154185359dup GRCh37
NC_000023.9:g.153838550_153838553dup NCBI36
NG_011403.1:g.70641_70644dup
NG_011403.2:g.70641_70644dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1626_1629dup MANE Select ENSP00000353393.4:p.Asp544IlefsTer12
ENST00000647125.1:c.*1502_*1505dup ENSP00000496062.1:n.*1502_*1505dup
ENST00000360256.8:c.1626_1629dup ENSP00000353393.4:p.Asp544IlefsTer12
NM_000132.3:c.1626_1629dup NP_000123.1:p.Asp544IlefsTer12
XM_011531126.1:c.1521_1524dup XP_011529428.1:p.Asp509IlefsTer12
NM_000132.4:c.1626_1629dup MANE Select NP_000123.1:p.Asp544IlefsTer12
Search 100 bp 5'
Search 100 bp 3'