Canonical Allele Identifier: CA2545796967

Gene: F7

Linked Data

• gnomAD v4: 13-113114037-CAGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113114038_113114040del , CM000675.2:g.113114038_113114040del	GRCh38
NC_000013.10:g.113768352_113768354del , CM000675.1:g.113768352_113768354del	GRCh37
NC_000013.9:g.112816353_112816355del	NCBI36
NG_009262.1:g.13248_13250del , LRG_554:g.13248_13250del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.364+78_364+80del MANE Select	ENSP00000329546.4:n.364+78_364+80del
ENST00000346342.7:c.364+78_364+80del	ENSP00000329546.3:n.364+78_364+80del
ENST00000375581.3:c.430+78_430+80del	ENSP00000364731.3:n.430+78_430+80del
ENST00000444337.1:c.*172+78_*172+80del	ENSP00000387669.1:n.*172+78_*172+80del
ENST00000473085.1:n.311+78_311+80del
ENST00000479674.1:n.697+78_697+80del
ENST00000541084.5:c.178+78_178+80del	ENSP00000442051.2:n.178+78_178+80del
NM_000131.4:c.430+78_430+80del , LRG_554t1:c.430+78_430+80del	NP_000122.1:n.430+78_430+80del
NM_001267554.1:c.178+78_178+80del	NP_001254483.1:n.178+78_178+80del
NM_019616.3:c.364+78_364+80del , LRG_554t2:c.364+78_364+80del	NP_062562.1:n.364+78_364+80del
NR_051961.1:n.451+78_451+80del
XM_006719963.2:c.364+78_364+80del	XP_006720026.1:n.364+78_364+80del
XM_011537474.1:c.364+78_364+80del	XP_011535776.1:n.364+78_364+80del
XM_011537475.1:c.178+78_178+80del	XP_011535777.1:n.178+78_178+80del
XM_011537477.1:c.325+78_325+80del	XP_011535779.1:n.325+78_325+80del
XM_006719963.3:c.409+78_409+80del	XP_006720026.2:n.409+78_409+80del
XM_011537474.2:c.409+78_409+80del	XP_011535776.2:n.409+78_409+80del
XM_011537475.2:c.223+78_223+80del	XP_011535777.2:n.223+78_223+80del
XM_011537476.2:c.-731_-729del	XP_011535778.1:n.-731_-729del
NM_019616.4:c.364+78_364+80del MANE Select	NP_062562.1:n.364+78_364+80del
NR_051961.2:n.448+78_448+80del
NM_001267554.2:c.178+78_178+80del	NP_001254483.1:n.178+78_178+80del