Canonical Allele Identifier: CA2695167719
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860544_154860547dup , CM000685.2:g.154860544_154860547dup GRCh38
NC_000023.10:g.154088819_154088822dup , CM000685.1:g.154088819_154088822dup GRCh37
NC_000023.9:g.153742013_153742016dup NCBI36
NG_011403.1:g.167179_167182dup
NG_011403.2:g.167179_167182dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6787_6790dup MANE Select ENSP00000353393.4:p.Thr2264AsnfsTer?
ENST00000644698.1:c.520_523dup ENSP00000495706.1:p.Thr175AsnfsTer?
ENST00000330287.10:c.382_385dup ENSP00000327895.6:p.Thr129AsnfsTer?
ENST00000360256.8:c.6787_6790dup ENSP00000353393.4:p.Thr2264AsnfsTer?
NM_000132.3:c.6787_6790dup NP_000123.1:p.Thr2264AsnfsTer?
NM_019863.2:c.382_385dup NP_063916.1:p.Thr129AsnfsTer?
XM_011531126.1:c.6682_6685dup XP_011529428.1:p.Thr2229AsnfsTer?
NM_000132.4:c.6787_6790dup MANE Select NP_000123.1:p.Thr2264AsnfsTer?
NM_019863.3:c.382_385dup NP_063916.1:p.Thr129AsnfsTer?