Canonical Allele Identifier: CA2120140698

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149404_113149418delinsTACACCAAGGTCACC , CM000675.2:g.113149404_113149418delinsTACACCAAGGTCACC	GRCh38
NC_000013.10:g.113803718_113803732delinsTACACCAAGGTCACC , CM000675.1:g.113803718_113803732delinsTACACCAAGGTCACC	GRCh37
NC_000013.9:g.112851719_112851733delinsTACACCAAGGTCACC	NCBI36
NG_009258.1:g.31606_31620delinsTACACCAAGGTCACC , LRG_548:g.31606_31620delinsTACACCAAGGTCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1354_1368delinsTACACCAAGGTCACC MANE Select	ENSP00000364709.3:p.Tyr452=
ENST00000375551.7:c.*345_*359delinsTACACCAAGGTCACC	ENSP00000364701.3:n.*345_*359delinsTACACCAAGGTCACC
ENST00000375559.7:c.1354_1368delinsTACACCAAGGTCACC	ENSP00000364709.3:p.Tyr452=
ENST00000409306.5:c.*345_*359delinsTACACCAAGGTCACC	ENSP00000387092.1:n.*345_*359delinsTACACCAAGGTCACC
NM_000504.3:c.1354_1368delinsTACACCAAGGTCACC , LRG_548t1:c.1354_1368delinsTACACCAAGGTCACC	NP_000495.1:p.Tyr452=
NM_001312674.1:c.1222_1236delinsTACACCAAGGTCACC	NP_001299603.1:p.Tyr408=
NM_001312675.1:c.*345_*359delinsTACACCAAGGTCACC	NP_001299604.1:n.*345_*359delinsTACACCAAGGTCACC
NM_000504.4:c.1354_1368delinsTACACCAAGGTCACC MANE Select	NP_000495.1:p.Tyr452=
NM_001312674.2:c.1222_1236delinsTACACCAAGGTCACC	NP_001299603.1:p.Tyr408=
NM_001312675.2:c.*345_*359delinsTACACCAAGGTCACC	NP_001299604.1:n.*345_*359delinsTACACCAAGGTCACC