Canonical Allele Identifier: CA2505074126
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954075_154954076dup , CM000685.2:g.154954075_154954076dup GRCh38
NC_000023.10:g.154182350_154182351dup , CM000685.1:g.154182350_154182351dup GRCh37
NC_000023.9:g.153835544_153835545dup NCBI36
NG_011403.1:g.73649_73650dup
NG_011403.2:g.73649_73650dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1753-33_1753-32dup MANE Select ENSP00000353393.4:n.1753-33_1753-32dup
ENST00000647125.1:c.*1629-33_*1629-32dup ENSP00000496062.1:n.*1629-33_*1629-32dup
ENST00000360256.8:c.1753-33_1753-32dup ENSP00000353393.4:n.1753-33_1753-32dup
NM_000132.3:c.1753-33_1753-32dup NP_000123.1:n.1753-33_1753-32dup
XM_011531126.1:c.1648-33_1648-32dup XP_011529428.1:n.1648-33_1648-32dup
NM_000132.4:c.1753-33_1753-32dup MANE Select NP_000123.1:n.1753-33_1753-32dup