Canonical Allele Identifier: CA2623811577

Gene: F7

Linked Data

• gnomAD v4: 13-113119912-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119917del , CM000675.2:g.113119917del	GRCh38
NC_000013.10:g.113774231del , CM000675.1:g.113774231del	GRCh37
NC_000013.9:g.112822232del	NCBI36
NG_009258.1:g.2119del , LRG_548:g.2119del
NG_009262.1:g.19127del , LRG_554:g.19127del

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.*909del MANE Select	ENSP00000329546.4:n.*909del
ENST00000346342.7:c.*909del	ENSP00000329546.3:n.*909del
ENST00000375581.3:c.*909del	ENSP00000364731.3:n.*909del
ENST00000541084.5:c.*909del	ENSP00000442051.2:n.*909del
NM_000131.4:c.*909del , LRG_554t1:c.*909del	NP_000122.1:n.*909del
NM_001267554.1:c.*909del	NP_001254483.1:n.*909del
NM_019616.3:c.*909del , LRG_554t2:c.*909del	NP_062562.1:n.*909del
NR_051961.1:n.2331del
XM_006719963.2:c.*909del	XP_006720026.1:n.*909del
XM_011537474.1:c.*909del	XP_011535776.1:n.*909del
XM_011537475.1:c.*909del	XP_011535777.1:n.*909del
XM_011537476.1:c.*909del	XP_011535778.1:n.*909del
XM_011537477.1:c.*909del	XP_011535779.1:n.*909del
XM_006719963.3:c.*909del	XP_006720026.2:n.*909del
XM_011537474.2:c.*909del	XP_011535776.2:n.*909del
XM_011537475.2:c.*909del	XP_011535777.2:n.*909del
XM_011537476.2:c.*909del	XP_011535778.1:n.*909del
NM_019616.4:c.*909del MANE Select	NP_062562.1:n.*909del
NR_051961.2:n.2328del
NM_001267554.2:c.*909del	NP_001254483.1:n.*909del