Canonical Allele Identifier: CA960394733

Gene: F7

Linked Data

• dbSNP Id: rs2036145890
• gnomAD v3: 13-113113773-AGTG-A
• gnomAD v4: 13-113113773-AGTG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113777_113113779del , CM000675.2:g.113113777_113113779del	GRCh38
NC_000013.10:g.113768091_113768093del , CM000675.1:g.113768091_113768093del	GRCh37
NC_000013.9:g.112816092_112816094del	NCBI36
NG_009262.1:g.12987_12989del , LRG_554:g.12987_12989del

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.250+1_250+3del
ENST00000346342.7:c.250+1_250+3del
ENST00000375581.3:c.316+1_316+3del
ENST00000444337.1:c.214_216del
ENST00000473085.1:n.197+1_197+3del
ENST00000479674.1:n.514_516del
ENST00000541084.5:c.65-70_65-68del	ENSP00000442051.2:n.65-70_65-68del
NM_000131.4:c.316+1_316+3del , LRG_554t1:c.316+1_316+3del
NM_001267554.1:c.65-70_65-68del	NP_001254483.1:n.65-70_65-68del
NM_019616.3:c.250+1_250+3del , LRG_554t2:c.250+1_250+3del
NR_051961.1:n.268_270del
XM_006719963.2:c.250+1_250+3del
XM_011537474.1:c.250+1_250+3del
XM_011537475.1:c.65-70_65-68del	XP_011535777.1:n.65-70_65-68del
XM_011537477.1:c.212-70_212-68del	XP_011535779.1:n.212-70_212-68del
XM_006719963.3:c.295+1_295+3del
XM_011537474.2:c.295+1_295+3del
XM_011537475.2:c.110-70_110-68del	XP_011535777.2:n.110-70_110-68del
NM_019616.4:c.250+1_250+3del
NR_051961.2:n.265_267del
NM_001267554.2:c.65-70_65-68del	NP_001254483.1:n.65-70_65-68del