Canonical Allele Identifier: CA612690894

Gene: F7

Linked Data

• dbSNP Id: rs1276719317
• gnomAD v2: 13-113773790-A-AATGCACACACACAGAGAT
• gnomAD v3: 13-113119476-A-AATGCACACACACAGAGAT
• gnomAD v4: 13-113119476-A-AATGCACACACACAGAGAT
• MyVariant Identifiers: chr13:g.113773790_113773791insATGCACACACACAGAGAT (hg19) ; chr13:g.113119476_113119477insATGCACACACACAGAGAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119489_113119506dup , CM000675.2:g.113119489_113119506dup	GRCh38
NC_000013.10:g.113773803_113773820dup , CM000675.1:g.113773803_113773820dup	GRCh37
NC_000013.9:g.112821804_112821821dup	NCBI36
NG_009258.1:g.1691_1708dup , LRG_548:g.1691_1708dup
NG_009262.1:g.18699_18716dup , LRG_554:g.18699_18716dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*481_*498dup MANE Select	ENSP00000329546.4:n.*481_*498dup
ENST00000346342.7:c.*481_*498dup	ENSP00000329546.3:n.*481_*498dup
ENST00000375581.3:c.*481_*498dup	ENSP00000364731.3:n.*481_*498dup
ENST00000541084.5:c.*481_*498dup	ENSP00000442051.2:n.*481_*498dup
NM_000131.4:c.*481_*498dup , LRG_554t1:c.*481_*498dup	NP_000122.1:n.*481_*498dup
NM_001267554.1:c.*481_*498dup	NP_001254483.1:n.*481_*498dup
NM_019616.3:c.*481_*498dup , LRG_554t2:c.*481_*498dup	NP_062562.1:n.*481_*498dup
NR_051961.1:n.1903_1920dup
XM_006719963.2:c.*481_*498dup	XP_006720026.1:n.*481_*498dup
XM_011537474.1:c.*481_*498dup	XP_011535776.1:n.*481_*498dup
XM_011537475.1:c.*481_*498dup	XP_011535777.1:n.*481_*498dup
XM_011537476.1:c.*481_*498dup	XP_011535778.1:n.*481_*498dup
XM_011537477.1:c.*481_*498dup	XP_011535779.1:n.*481_*498dup
XM_006719963.3:c.*481_*498dup	XP_006720026.2:n.*481_*498dup
XM_011537474.2:c.*481_*498dup	XP_011535776.2:n.*481_*498dup
XM_011537475.2:c.*481_*498dup	XP_011535777.2:n.*481_*498dup
XM_011537476.2:c.*481_*498dup	XP_011535778.1:n.*481_*498dup
NM_019616.4:c.*481_*498dup MANE Select	NP_062562.1:n.*481_*498dup
NR_051961.2:n.1900_1917dup
NM_001267554.2:c.*481_*498dup	NP_001254483.1:n.*481_*498dup