Canonical Allele Identifier: CA612868380

Gene: F10

Linked Data

• gnomAD v2: 13-113803690-CTGT-C
• gnomAD v3: 13-113149376-CTGT-C
• gnomAD v4: 13-113149376-CTGT-C
• MyVariant Identifiers: chr13:g.113803691_113803693del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149377_113149379del , CM000675.2:g.113149377_113149379del	GRCh38
NC_000013.10:g.113803691_113803693del , CM000675.1:g.113803691_113803693del	GRCh37
NC_000013.9:g.112851692_112851694del	NCBI36
NG_009258.1:g.31579_31581del , LRG_548:g.31579_31581del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1327_1329del MANE Select	ENSP00000364709.3:p.Cys443del
ENST00000375551.7:c.*318_*320del	ENSP00000364701.3:n.*318_*320del
ENST00000375559.7:c.1327_1329del	ENSP00000364709.3:p.Cys443del
ENST00000409306.5:c.*318_*320del	ENSP00000387092.1:n.*318_*320del
NM_000504.3:c.1327_1329del , LRG_548t1:c.1327_1329del	NP_000495.1:p.Cys443del
NM_001312674.1:c.1195_1197del	NP_001299603.1:p.Cys399del
NM_001312675.1:c.*318_*320del	NP_001299604.1:n.*318_*320del
NM_000504.4:c.1327_1329del MANE Select	NP_000495.1:p.Cys443del
NM_001312674.2:c.1195_1197del	NP_001299603.1:p.Cys399del
NM_001312675.2:c.*318_*320del	NP_001299604.1:n.*318_*320del