Canonical Allele Identifier: CA2120140429

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149297_113149298delinsAG , CM000675.2:g.113149297_113149298delinsAG	GRCh38
NC_000013.10:g.113803611_113803612delinsAG , CM000675.1:g.113803611_113803612delinsAG	GRCh37
NC_000013.9:g.112851612_112851613delinsAG	NCBI36
NG_009258.1:g.31499_31500delinsAG , LRG_548:g.31499_31500delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1247_1248delinsAG MANE Select	ENSP00000364709.3:p.Gln416=
ENST00000375551.7:c.*238_*239delinsAG	ENSP00000364701.3:n.*238_*239delinsAG
ENST00000375559.7:c.1247_1248delinsAG	ENSP00000364709.3:p.Gln416=
ENST00000409306.5:c.*238_*239delinsAG	ENSP00000387092.1:n.*238_*239delinsAG
NM_000504.3:c.1247_1248delinsAG , LRG_548t1:c.1247_1248delinsAG	NP_000495.1:p.Gln416=
NM_001312674.1:c.1115_1116delinsAG	NP_001299603.1:p.Gln372=
NM_001312675.1:c.*238_*239delinsAG	NP_001299604.1:n.*238_*239delinsAG
NM_000504.4:c.1247_1248delinsAG MANE Select	NP_000495.1:p.Gln416=
NM_001312674.2:c.1115_1116delinsAG	NP_001299603.1:p.Gln372=
NM_001312675.2:c.*238_*239delinsAG	NP_001299604.1:n.*238_*239delinsAG