Canonical Allele Identifier: CA256462418

Gene: F7

Linked Data

• dbSNP Id: rs904016206
• gnomAD v4: 13-113119511-GCA-G
• MyVariant Identifiers: chr13:g.113773826_113773827del (hg19) ; chr13:g.113119512_113119513del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119518_113119519del , CM000675.2:g.113119518_113119519del	GRCh38
NC_000013.10:g.113773832_113773833del , CM000675.1:g.113773832_113773833del	GRCh37
NC_000013.9:g.112821833_112821834del	NCBI36
NG_009258.1:g.1720_1721del , LRG_548:g.1720_1721del
NG_009262.1:g.18728_18729del , LRG_554:g.18728_18729del

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.*510_*511del MANE Select	ENSP00000329546.4:n.*510_*511del
ENST00000346342.7:c.*510_*511del	ENSP00000329546.3:n.*510_*511del
ENST00000375581.3:c.*510_*511del	ENSP00000364731.3:n.*510_*511del
ENST00000541084.5:c.*510_*511del	ENSP00000442051.2:n.*510_*511del
NM_000131.4:c.*510_*511del , LRG_554t1:c.*510_*511del	NP_000122.1:n.*510_*511del
NM_001267554.1:c.*510_*511del	NP_001254483.1:n.*510_*511del
NM_019616.3:c.*510_*511del , LRG_554t2:c.*510_*511del	NP_062562.1:n.*510_*511del
NR_051961.1:n.1932_1933del
XM_006719963.2:c.*510_*511del	XP_006720026.1:n.*510_*511del
XM_011537474.1:c.*510_*511del	XP_011535776.1:n.*510_*511del
XM_011537475.1:c.*510_*511del	XP_011535777.1:n.*510_*511del
XM_011537476.1:c.*510_*511del	XP_011535778.1:n.*510_*511del
XM_011537477.1:c.*510_*511del	XP_011535779.1:n.*510_*511del
XM_006719963.3:c.*510_*511del	XP_006720026.2:n.*510_*511del
XM_011537474.2:c.*510_*511del	XP_011535776.2:n.*510_*511del
XM_011537475.2:c.*510_*511del	XP_011535777.2:n.*510_*511del
XM_011537476.2:c.*510_*511del	XP_011535778.1:n.*510_*511del
NM_019616.4:c.*510_*511del MANE Select	NP_062562.1:n.*510_*511del
NR_051961.2:n.1929_1930del
NM_001267554.2:c.*510_*511del	NP_001254483.1:n.*510_*511del