Canonical Allele Identifier: CA2623810415

Gene: F10

Linked Data

• gnomAD v4: 13-113149455-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149459del , CM000675.2:g.113149459del	GRCh38
NC_000013.10:g.113803773del , CM000675.1:g.113803773del	GRCh37
NC_000013.9:g.112851774del	NCBI36
NG_009258.1:g.31661del , LRG_548:g.31661del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1409del MANE Select	ENSP00000364709.3:p.Gly470AlafsTer13
ENST00000375551.7:c.*400del	ENSP00000364701.3:n.*400del
ENST00000375559.7:c.1409del	ENSP00000364709.3:p.Gly470AlafsTer13
ENST00000409306.5:c.*400del	ENSP00000387092.1:n.*400del
NM_000504.3:c.1409del , LRG_548t1:c.1409del	NP_000495.1:p.Gly470AlafsTer13
NM_001312674.1:c.1277del	NP_001299603.1:p.Gly426AlafsTer13
NM_001312675.1:c.*400del	NP_001299604.1:n.*400del
NM_000504.4:c.1409del MANE Select	NP_000495.1:p.Gly470AlafsTer13
NM_001312674.2:c.1277del	NP_001299603.1:p.Gly426AlafsTer13
NM_001312675.2:c.*400del	NP_001299604.1:n.*400del