Canonical Allele Identifier: CA2695167345
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837513del , CM000685.2:g.154837513del GRCh38
NC_000023.10:g.154065788del , CM000685.1:g.154065788del GRCh37
NC_000023.9:g.153718982del NCBI36
NG_011403.1:g.190212del
NG_033065.1:g.2151del
NG_011403.2:g.190212del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*85del MANE Select ENSP00000353393.4:n.*85del
ENST00000644698.1:c.*85del ENSP00000495706.1:n.*85del
ENST00000330287.10:c.*85del ENSP00000327895.6:n.*85del
ENST00000360256.8:c.*85del ENSP00000353393.4:n.*85del
NM_000132.3:c.*85del NP_000123.1:n.*85del
NM_019863.2:c.*85del NP_063916.1:n.*85del
XM_011531126.1:c.*85del XP_011529428.1:n.*85del
NM_000132.4:c.*85del MANE Select NP_000123.1:n.*85del
NM_019863.3:c.*85del NP_063916.1:n.*85del