Canonical Allele Identifier: CA2695152092
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896312_154896316del , CM000685.2:g.154896312_154896316del GRCh38
NC_000023.10:g.154124587_154124591del , CM000685.1:g.154124587_154124591del GRCh37
NC_000023.9:g.153777781_153777785del NCBI36
NG_011403.1:g.131408_131412del
NG_011403.2:g.131408_131412del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6274-84_6274-80del MANE Select ENSP00000353393.4:n.6274-84_6274-80del
ENST00000360256.8:c.6274-84_6274-80del ENSP00000353393.4:n.6274-84_6274-80del
NM_000132.3:c.6274-84_6274-80del NP_000123.1:n.6274-84_6274-80del
XM_011531126.1:c.6169-84_6169-80del XP_011529428.1:n.6169-84_6169-80del
NM_000132.4:c.6274-84_6274-80del MANE Select NP_000123.1:n.6274-84_6274-80del