Canonical Allele Identifier: CA2623808384

Gene: F10

Linked Data

• gnomAD v4: 13-113139551-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113139551C>T , CM000675.2:g.113139551C>T	GRCh38
NC_000013.10:g.113793865C>T , CM000675.1:g.113793865C>T	GRCh37
NC_000013.9:g.112841866C>T	NCBI36
NG_009258.1:g.21753C>T , LRG_548:g.21753C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375559.8:c.370+81C>T MANE Select	ENSP00000364709.3:n.370+81C>T
ENST00000375551.7:c.370+81C>T	ENSP00000364701.3:n.370+81C>T
ENST00000375559.7:c.370+81C>T	ENSP00000364709.3:n.370+81C>T
ENST00000409306.5:c.370+81C>T	ENSP00000387092.1:n.370+81C>T
ENST00000410083.6:c.370+81C>T	ENSP00000386320.2:n.370+81C>T
ENST00000477269.5:n.407+81C>T
NM_000504.3:c.370+81C>T , LRG_548t1:c.370+81C>T	NP_000495.1:n.370+81C>T
NM_001312674.1:c.370+81C>T	NP_001299603.1:n.370+81C>T
NM_001312675.1:c.370+81C>T	NP_001299604.1:n.370+81C>T
NM_000504.4:c.370+81C>T MANE Select	NP_000495.1:n.370+81C>T
NM_001312674.2:c.370+81C>T	NP_001299603.1:n.370+81C>T
NM_001312675.2:c.370+81C>T	NP_001299604.1:n.370+81C>T