Canonical Allele Identifier: CA2800665264

Gene: F10

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149369_113149370insTTTTTTTTTTTAATG , CM000675.2:g.113149369_113149370insTTTTTTTTTTTAATG	GRCh38
NC_000013.10:g.113803683_113803684insTTTTTTTTTTTAATG , CM000675.1:g.113803683_113803684insTTTTTTTTTTTAATG	GRCh37
NC_000013.9:g.112851684_112851685insTTTTTTTTTTTAATG	NCBI36
NG_009258.1:g.31571_31572insTTTTTTTTTTTAATG , LRG_548:g.31571_31572insTTTTTTTTTTTAATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1319_1320insTTTTTTTTTTTAATG MANE Select	ENSP00000364709.3:p.Gly441PhefsTer4
ENST00000375551.7:c.*310_*311insTTTTTTTTTTTAATG	ENSP00000364701.3:n.*310_*311insTTTTTTTTTTTAATG
ENST00000375559.7:c.1319_1320insTTTTTTTTTTTAATG	ENSP00000364709.3:p.Gly441PhefsTer4
ENST00000409306.5:c.*310_*311insTTTTTTTTTTTAATG	ENSP00000387092.1:n.*310_*311insTTTTTTTTTTTAATG
NM_000504.3:c.1319_1320insTTTTTTTTTTTAATG , LRG_548t1:c.1319_1320insTTTTTTTTTTTAATG	NP_000495.1:p.Gly441PhefsTer4
NM_001312674.1:c.1187_1188insTTTTTTTTTTTAATG	NP_001299603.1:p.Gly397PhefsTer4
NM_001312675.1:c.*310_*311insTTTTTTTTTTTAATG	NP_001299604.1:n.*310_*311insTTTTTTTTTTTAATG
NM_000504.4:c.1319_1320insTTTTTTTTTTTAATG MANE Select	NP_000495.1:p.Gly441PhefsTer4
NM_001312674.2:c.1187_1188insTTTTTTTTTTTAATG	NP_001299603.1:p.Gly397PhefsTer4
NM_001312675.2:c.*310_*311insTTTTTTTTTTTAATG	NP_001299604.1:n.*310_*311insTTTTTTTTTTTAATG