Canonical Allele Identifier: CA612868379

Gene: F10

Linked Data

• dbSNP Id: rs1404274268
• gnomAD v2: 13-113803687-GGGC-G
• gnomAD v3: 13-113149373-GGGC-G
• gnomAD v4: 13-113149373-GGGC-G
• MyVariant Identifiers: chr13:g.113803688_113803690del (hg19) ; chr13:g.113149374_113149376del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149374_113149376del , CM000675.2:g.113149374_113149376del	GRCh38
NC_000013.10:g.113803688_113803690del , CM000675.1:g.113803688_113803690del	GRCh37
NC_000013.9:g.112851689_112851691del	NCBI36
NG_009258.1:g.31576_31578del , LRG_548:g.31576_31578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1324_1326del MANE Select	ENSP00000364709.3:p.Gly442del
ENST00000375551.7:c.*315_*317del	ENSP00000364701.3:n.*315_*317del
ENST00000375559.7:c.1324_1326del	ENSP00000364709.3:p.Gly442del
ENST00000409306.5:c.*315_*317del	ENSP00000387092.1:n.*315_*317del
NM_000504.3:c.1324_1326del , LRG_548t1:c.1324_1326del	NP_000495.1:p.Gly442del
NM_001312674.1:c.1192_1194del	NP_001299603.1:p.Gly398del
NM_001312675.1:c.*315_*317del	NP_001299604.1:n.*315_*317del
NM_000504.4:c.1324_1326del MANE Select	NP_000495.1:p.Gly442del
NM_001312674.2:c.1192_1194del	NP_001299603.1:p.Gly398del
NM_001312675.2:c.*315_*317del	NP_001299604.1:n.*315_*317del