Canonical Allele Identifier: CA7060729

Gene: F10

Linked Data

• dbSNP Id: rs762062267
• ExAC: 13:113803690 C / G
• gnomAD v2: 13-113803690-C-G
• gnomAD v3: 13-113149376-C-G
• gnomAD v4: 13-113149376-C-G
• MyVariant Identifiers: chr13:g.113803690C>G (hg19) ; chr13:g.113803690_113803693delinsGTGT (hg19) ; chr13:g.113149376C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113149376C>G , CM000675.2:g.113149376C>G	GRCh38
NC_000013.10:g.113803690C>G , CM000675.1:g.113803690C>G	GRCh37
NC_000013.9:g.112851691C>G	NCBI36
NG_009258.1:g.31578C>G , LRG_548:g.31578C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375559.8:c.1326C>G MANE Select	ENSP00000364709.3:p.Gly442=
ENST00000375551.7:c.*317C>G	ENSP00000364701.3:n.*317C>G
ENST00000375559.7:c.1326C>G	ENSP00000364709.3:p.Gly442=
ENST00000409306.5:c.*317C>G	ENSP00000387092.1:n.*317C>G
NM_000504.3:c.1326C>G , LRG_548t1:c.1326C>G	NP_000495.1:p.Gly442=
NM_001312674.1:c.1194C>G	NP_001299603.1:p.Gly398=
NM_001312675.1:c.*317C>G	NP_001299604.1:n.*317C>G
NM_000504.4:c.1326C>G MANE Select	NP_000495.1:p.Gly442=
NM_001312674.2:c.1194C>G	NP_001299603.1:p.Gly398=
NM_001312675.2:c.*317C>G	NP_001299604.1:n.*317C>G