Canonical Allele Identifier: CA695282668

Gene: F7

Linked Data

• dbSNP Id: rs1320672573
• MyVariant Identifiers: chr13:g.113768337_113768346del (hg19) ; chr13:g.113114023_113114032del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113114024_113114033del , CM000675.2:g.113114024_113114033del	GRCh38
NC_000013.10:g.113768338_113768347del , CM000675.1:g.113768338_113768347del	GRCh37
NC_000013.9:g.112816339_112816348del	NCBI36
NG_009262.1:g.13234_13243del , LRG_554:g.13234_13243del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364+64_364+73del MANE Select	ENSP00000329546.4:n.364+64_364+73del
ENST00000346342.7:c.364+64_364+73del	ENSP00000329546.3:n.364+64_364+73del
ENST00000375581.3:c.430+64_430+73del	ENSP00000364731.3:n.430+64_430+73del
ENST00000444337.1:c.*172+64_*172+73del	ENSP00000387669.1:n.*172+64_*172+73del
ENST00000473085.1:n.311+64_311+73del
ENST00000479674.1:n.697+64_697+73del
ENST00000541084.5:c.178+64_178+73del	ENSP00000442051.2:n.178+64_178+73del
NM_000131.4:c.430+64_430+73del , LRG_554t1:c.430+64_430+73del	NP_000122.1:n.430+64_430+73del
NM_001267554.1:c.178+64_178+73del	NP_001254483.1:n.178+64_178+73del
NM_019616.3:c.364+64_364+73del , LRG_554t2:c.364+64_364+73del	NP_062562.1:n.364+64_364+73del
NR_051961.1:n.451+64_451+73del
XM_006719963.2:c.364+64_364+73del	XP_006720026.1:n.364+64_364+73del
XM_011537474.1:c.364+64_364+73del	XP_011535776.1:n.364+64_364+73del
XM_011537475.1:c.178+64_178+73del	XP_011535777.1:n.178+64_178+73del
XM_011537477.1:c.325+64_325+73del	XP_011535779.1:n.325+64_325+73del
XM_006719963.3:c.409+64_409+73del	XP_006720026.2:n.409+64_409+73del
XM_011537474.2:c.409+64_409+73del	XP_011535776.2:n.409+64_409+73del
XM_011537475.2:c.223+64_223+73del	XP_011535777.2:n.223+64_223+73del
XM_011537476.2:c.-745_-736del	XP_011535778.1:n.-745_-736del
NM_019616.4:c.364+64_364+73del MANE Select	NP_062562.1:n.364+64_364+73del
NR_051961.2:n.448+64_448+73del
NM_001267554.2:c.178+64_178+73del	NP_001254483.1:n.178+64_178+73del