Canonical Allele Identifier: CA2623810347

Gene: F10

Linked Data

• gnomAD v4: 13-113149399-G-GCGACCTCCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149399_113149400insCGACCTCCGA , CM000675.2:g.113149399_113149400insCGACCTCCGA	GRCh38
NC_000013.10:g.113803713_113803714insCGACCTCCGA , CM000675.1:g.113803713_113803714insCGACCTCCGA	GRCh37
NC_000013.9:g.112851714_112851715insCGACCTCCGA	NCBI36
NG_009258.1:g.31601_31602insCGACCTCCGA , LRG_548:g.31601_31602insCGACCTCCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1349_1350insCGACCTCCGA MANE Select	ENSP00000364709.3:p.Ile451AspfsTer?
ENST00000375551.7:c.*340_*341insCGACCTCCGA	ENSP00000364701.3:n.*340_*341insCGACCTCCGA
ENST00000375559.7:c.1349_1350insCGACCTCCGA	ENSP00000364709.3:p.Ile451AspfsTer?
ENST00000409306.5:c.*340_*341insCGACCTCCGA	ENSP00000387092.1:n.*340_*341insCGACCTCCGA
NM_000504.3:c.1349_1350insCGACCTCCGA , LRG_548t1:c.1349_1350insCGACCTCCGA	NP_000495.1:p.Ile451AspfsTer?
NM_001312674.1:c.1217_1218insCGACCTCCGA	NP_001299603.1:p.Ile407AspfsTer?
NM_001312675.1:c.*340_*341insCGACCTCCGA	NP_001299604.1:n.*340_*341insCGACCTCCGA
NM_000504.4:c.1349_1350insCGACCTCCGA MANE Select	NP_000495.1:p.Ile451AspfsTer?
NM_001312674.2:c.1217_1218insCGACCTCCGA	NP_001299603.1:p.Ile407AspfsTer?
NM_001312675.2:c.*340_*341insCGACCTCCGA	NP_001299604.1:n.*340_*341insCGACCTCCGA