Canonical Allele Identifier: CA2623809560
Gene: F10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113149075_113149078dup , CM000675.2:g.113149075_113149078dup GRCh38
NC_000013.10:g.113803389_113803392dup , CM000675.1:g.113803389_113803392dup GRCh37
NC_000013.9:g.112851390_112851393dup NCBI36
NG_009258.1:g.31277_31280dup , LRG_548:g.31277_31280dup

Transcript Alleles

HGVS Amino-acid change
ENST00000375559.8:c.1025_1028dup MANE Select ENSP00000364709.3:p.Glu345ProfsTer4
ENST00000375551.7:c.*16_*19dup ENSP00000364701.3:n.*16_*19dup
ENST00000375559.7:c.1025_1028dup ENSP00000364709.3:p.Glu345ProfsTer4
ENST00000409306.5:c.*16_*19dup ENSP00000387092.1:n.*16_*19dup
NM_000504.3:c.1025_1028dup , LRG_548t1:c.1025_1028dup NP_000495.1:p.Glu345ProfsTer4
NM_001312674.1:c.893_896dup NP_001299603.1:p.Glu301ProfsTer4
NM_001312675.1:c.*16_*19dup NP_001299604.1:n.*16_*19dup
NM_000504.4:c.1025_1028dup MANE Select NP_000495.1:p.Glu345ProfsTer4
NM_001312674.2:c.893_896dup NP_001299603.1:p.Glu301ProfsTer4
NM_001312675.2:c.*16_*19dup NP_001299604.1:n.*16_*19dup