Canonical Allele Identifier: CA2623806929

Gene: F10 F10-AS1

Linked Data

• gnomAD v4: 13-113129638-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113129638T>C , CM000675.2:g.113129638T>C	GRCh38
NC_000013.10:g.113783952T>C , CM000675.1:g.113783952T>C	GRCh37
NC_000013.9:g.112831953T>C	NCBI36
NG_009258.1:g.11840T>C , LRG_548:g.11840T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.231+26T>C (F10) MANE Select	ENSP00000364709.3:n.231+26T>C
ENST00000375551.7:c.231+26T>C (F10)	ENSP00000364701.3:n.231+26T>C
ENST00000375559.7:c.231+26T>C (F10)	ENSP00000364709.3:n.231+26T>C
ENST00000409306.5:c.231+26T>C (F10)	ENSP00000387092.1:n.231+26T>C
ENST00000410083.6:c.231+26T>C (F10)	ENSP00000386320.2:n.231+26T>C
ENST00000477269.5:n.268+26T>C (F10)
ENST00000483537.1:n.251+26T>C (F10)
NM_000504.3:c.231+26T>C , LRG_548t1:c.231+26T>C (F10)	NP_000495.1:n.231+26T>C
NM_001312674.1:c.231+26T>C (F10)	NP_001299603.1:n.231+26T>C
NM_001312675.1:c.231+26T>C (F10)	NP_001299604.1:n.231+26T>C
NR_126424.1:n.41+368A>G (F10-AS1)
NM_000504.4:c.231+26T>C (F10) MANE Select	NP_000495.1:n.231+26T>C
NM_001312674.2:c.231+26T>C (F10)	NP_001299603.1:n.231+26T>C
NM_001312675.2:c.231+26T>C (F10)	NP_001299604.1:n.231+26T>C