Canonical Allele Identifier: CA2120143594
Gene: F7 HGNC NCBI

Linked Data

dbSNP Id: rs2036258479

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119282_113119287dup , CM000675.2:g.113119282_113119287dup GRCh38
NC_000013.10:g.113773596_113773601dup , CM000675.1:g.113773596_113773601dup GRCh37
NC_000013.9:g.112821597_112821602dup NCBI36
NG_009258.1:g.1484_1489dup , LRG_548:g.1484_1489dup
NG_009262.1:g.18492_18497dup , LRG_554:g.18492_18497dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.*274_*279dup MANE Select ENSP00000329546.4:n.*274_*279dup
ENST00000346342.7:c.*274_*279dup ENSP00000329546.3:n.*274_*279dup
ENST00000375581.3:c.*274_*279dup ENSP00000364731.3:n.*274_*279dup
ENST00000541084.5:c.*274_*279dup ENSP00000442051.2:n.*274_*279dup
NM_000131.4:c.*274_*279dup , LRG_554t1:c.*274_*279dup NP_000122.1:n.*274_*279dup
NM_001267554.1:c.*274_*279dup NP_001254483.1:n.*274_*279dup
NM_019616.3:c.*274_*279dup , LRG_554t2:c.*274_*279dup NP_062562.1:n.*274_*279dup
NR_051961.1:n.1696_1701dup
XM_006719963.2:c.*274_*279dup XP_006720026.1:n.*274_*279dup
XM_011537474.1:c.*274_*279dup XP_011535776.1:n.*274_*279dup
XM_011537475.1:c.*274_*279dup XP_011535777.1:n.*274_*279dup
XM_011537476.1:c.*274_*279dup XP_011535778.1:n.*274_*279dup
XM_011537477.1:c.*274_*279dup XP_011535779.1:n.*274_*279dup
XM_006719963.3:c.*274_*279dup XP_006720026.2:n.*274_*279dup
XM_011537474.2:c.*274_*279dup XP_011535776.2:n.*274_*279dup
XM_011537475.2:c.*274_*279dup XP_011535777.2:n.*274_*279dup
XM_011537476.2:c.*274_*279dup XP_011535778.1:n.*274_*279dup
NM_019616.4:c.*274_*279dup MANE Select NP_062562.1:n.*274_*279dup
NR_051961.2:n.1693_1698dup
NM_001267554.2:c.*274_*279dup NP_001254483.1:n.*274_*279dup