Canonical Allele Identifier: CA2623803750
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113114035_113114054dup , CM000675.2:g.113114035_113114054dup GRCh38
NC_000013.10:g.113768349_113768368dup , CM000675.1:g.113768349_113768368dup GRCh37
NC_000013.9:g.112816350_112816369dup NCBI36
NG_009262.1:g.13245_13264dup , LRG_554:g.13245_13264dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.364+75_364+94dup MANE Select ENSP00000329546.4:n.364+75_364+94dup
ENST00000346342.7:c.364+75_364+94dup ENSP00000329546.3:n.364+75_364+94dup
ENST00000375581.3:c.430+75_430+94dup ENSP00000364731.3:n.430+75_430+94dup
ENST00000444337.1:c.*172+75_*172+94dup ENSP00000387669.1:n.*172+75_*172+94dup
ENST00000473085.1:n.311+75_311+94dup
ENST00000479674.1:n.697+75_697+94dup
ENST00000541084.5:c.178+75_178+94dup ENSP00000442051.2:n.178+75_178+94dup
NM_000131.4:c.430+75_430+94dup , LRG_554t1:c.430+75_430+94dup NP_000122.1:n.430+75_430+94dup
NM_001267554.1:c.178+75_178+94dup NP_001254483.1:n.178+75_178+94dup
NM_019616.3:c.364+75_364+94dup , LRG_554t2:c.364+75_364+94dup NP_062562.1:n.364+75_364+94dup
NR_051961.1:n.451+75_451+94dup
XM_006719963.2:c.364+75_364+94dup XP_006720026.1:n.364+75_364+94dup
XM_011537474.1:c.364+75_364+94dup XP_011535776.1:n.364+75_364+94dup
XM_011537475.1:c.178+75_178+94dup XP_011535777.1:n.178+75_178+94dup
XM_011537477.1:c.325+75_325+94dup XP_011535779.1:n.325+75_325+94dup
XM_006719963.3:c.409+75_409+94dup XP_006720026.2:n.409+75_409+94dup
XM_011537474.2:c.409+75_409+94dup XP_011535776.2:n.409+75_409+94dup
XM_011537475.2:c.223+75_223+94dup XP_011535777.2:n.223+75_223+94dup
XM_011537476.2:c.-734_-715dup XP_011535778.1:n.-734_-715dup
NM_019616.4:c.364+75_364+94dup MANE Select NP_062562.1:n.364+75_364+94dup
NR_051961.2:n.448+75_448+94dup
NM_001267554.2:c.178+75_178+94dup NP_001254483.1:n.178+75_178+94dup