Canonical Allele Identifier: CA2695167393
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837568_154837582dup , CM000685.2:g.154837568_154837582dup GRCh38
NC_000023.10:g.154065843_154065857dup , CM000685.1:g.154065843_154065857dup GRCh37
NC_000023.9:g.153719037_153719051dup NCBI36
NG_011403.1:g.190143_190157dup
NG_033065.1:g.2082_2096dup
NG_011403.2:g.190143_190157dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*16_*30dup MANE Select ENSP00000353393.4:n.*16_*30dup
ENST00000644698.1:c.*16_*30dup ENSP00000495706.1:n.*16_*30dup
ENST00000330287.10:c.*16_*30dup ENSP00000327895.6:n.*16_*30dup
ENST00000360256.8:c.*16_*30dup ENSP00000353393.4:n.*16_*30dup
NM_000132.3:c.*16_*30dup NP_000123.1:n.*16_*30dup
NM_019863.2:c.*16_*30dup NP_063916.1:n.*16_*30dup
XM_011531126.1:c.*16_*30dup XP_011529428.1:n.*16_*30dup
NM_000132.4:c.*16_*30dup MANE Select NP_000123.1:n.*16_*30dup
NM_019863.3:c.*16_*30dup NP_063916.1:n.*16_*30dup