Canonical Allele Identifier: CA695269211

Gene: F7

Linked Data

• dbSNP Id: rs772137874
• gnomAD v3: 13-113119479-GCA-G
• gnomAD v4: 13-113119479-GCA-G
• MyVariant Identifiers: chr13:g.113773794_113773795del (hg19) ; chr13:g.113119480_113119481del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119488_113119489del , CM000675.2:g.113119488_113119489del	GRCh38
NC_000013.10:g.113773802_113773803del , CM000675.1:g.113773802_113773803del	GRCh37
NC_000013.9:g.112821803_112821804del	NCBI36
NG_009258.1:g.1690_1691del , LRG_548:g.1690_1691del
NG_009262.1:g.18698_18699del , LRG_554:g.18698_18699del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*480_*481del MANE Select	ENSP00000329546.4:n.*480_*481del
ENST00000346342.7:c.*480_*481del	ENSP00000329546.3:n.*480_*481del
ENST00000375581.3:c.*480_*481del	ENSP00000364731.3:n.*480_*481del
ENST00000541084.5:c.*480_*481del	ENSP00000442051.2:n.*480_*481del
NM_000131.4:c.*480_*481del , LRG_554t1:c.*480_*481del	NP_000122.1:n.*480_*481del
NM_001267554.1:c.*480_*481del	NP_001254483.1:n.*480_*481del
NM_019616.3:c.*480_*481del , LRG_554t2:c.*480_*481del	NP_062562.1:n.*480_*481del
NR_051961.1:n.1902_1903del
XM_006719963.2:c.*480_*481del	XP_006720026.1:n.*480_*481del
XM_011537474.1:c.*480_*481del	XP_011535776.1:n.*480_*481del
XM_011537475.1:c.*480_*481del	XP_011535777.1:n.*480_*481del
XM_011537476.1:c.*480_*481del	XP_011535778.1:n.*480_*481del
XM_011537477.1:c.*480_*481del	XP_011535779.1:n.*480_*481del
XM_006719963.3:c.*480_*481del	XP_006720026.2:n.*480_*481del
XM_011537474.2:c.*480_*481del	XP_011535776.2:n.*480_*481del
XM_011537475.2:c.*480_*481del	XP_011535777.2:n.*480_*481del
XM_011537476.2:c.*480_*481del	XP_011535778.1:n.*480_*481del
NM_019616.4:c.*480_*481del MANE Select	NP_062562.1:n.*480_*481del
NR_051961.2:n.1899_1900del
NM_001267554.2:c.*480_*481del	NP_001254483.1:n.*480_*481del