Canonical Allele Identifier: CA2695169054
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954051_154954052insG , CM000685.2:g.154954051_154954052insG GRCh38
NC_000023.10:g.154182326_154182327insG , CM000685.1:g.154182326_154182327insG GRCh37
NC_000023.9:g.153835520_153835521insG NCBI36
NG_011403.1:g.73672_73673insC
NG_011403.2:g.73672_73673insC

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1753-10_1753-9insC MANE Select ENSP00000353393.4:n.1753-10_1753-9insC
ENST00000647125.1:c.*1629-10_*1629-9insC ENSP00000496062.1:n.*1629-10_*1629-9insC
ENST00000360256.8:c.1753-10_1753-9insC ENSP00000353393.4:n.1753-10_1753-9insC
NM_000132.3:c.1753-10_1753-9insC NP_000123.1:n.1753-10_1753-9insC
XM_011531126.1:c.1648-10_1648-9insC XP_011529428.1:n.1648-10_1648-9insC
NM_000132.4:c.1753-10_1753-9insC MANE Select NP_000123.1:n.1753-10_1753-9insC