Canonical Allele Identifier: CA2623809558

Gene: F10

Linked Data

• gnomAD v4: 13-113149054-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149055del , CM000675.2:g.113149055del	GRCh38
NC_000013.10:g.113803369del , CM000675.1:g.113803369del	GRCh37
NC_000013.9:g.112851370del	NCBI36
NG_009258.1:g.31257del , LRG_548:g.31257del

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.1005del MANE Select	ENSP00000364709.3:p.Met336Ter
ENST00000375551.7:c.995del	ENSP00000364701.3:p.Ala332AspfsTer12
ENST00000375559.7:c.1005del	ENSP00000364709.3:p.Met336Ter
ENST00000409306.5:c.1001del	ENSP00000387092.1:p.Ala334AspfsTer12
NM_000504.3:c.1005del , LRG_548t1:c.1005del	NP_000495.1:p.Met336Ter
NM_001312674.1:c.873del	NP_001299603.1:p.Met292Ter
NM_001312675.1:c.995del	NP_001299604.1:p.Ala332AspfsTer12
NM_000504.4:c.1005del MANE Select	NP_000495.1:p.Met336Ter
NM_001312674.2:c.873del	NP_001299603.1:p.Met292Ter
NM_001312675.2:c.995del	NP_001299604.1:p.Ala332AspfsTer12