Canonical Allele Identifier: CA2623810225

Gene: F10

Linked Data

• gnomAD v4: 13-113149375-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149376del , CM000675.2:g.113149376del	GRCh38
NC_000013.10:g.113803690del , CM000675.1:g.113803690del	GRCh37
NC_000013.9:g.112851691del	NCBI36
NG_009258.1:g.31578del , LRG_548:g.31578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1326del MANE Select	ENSP00000364709.3:p.Cys443ValfsTer24
ENST00000375551.7:c.*317del	ENSP00000364701.3:n.*317del
ENST00000375559.7:c.1326del	ENSP00000364709.3:p.Cys443ValfsTer24
ENST00000409306.5:c.*317del	ENSP00000387092.1:n.*317del
NM_000504.3:c.1326del , LRG_548t1:c.1326del	NP_000495.1:p.Cys443ValfsTer24
NM_001312674.1:c.1194del	NP_001299603.1:p.Cys399ValfsTer24
NM_001312675.1:c.*317del	NP_001299604.1:n.*317del
NM_000504.4:c.1326del MANE Select	NP_000495.1:p.Cys443ValfsTer24
NM_001312674.2:c.1194del	NP_001299603.1:p.Cys399ValfsTer24
NM_001312675.2:c.*317del	NP_001299604.1:n.*317del