Canonical Allele Identifier: CA2623808611
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113118341G>T , CM000675.2:g.113118341G>T GRCh38
NC_000013.10:g.113772655G>T , CM000675.1:g.113772655G>T GRCh37
NC_000013.9:g.112820656G>T NCBI36
NG_009258.1:g.543G>T , LRG_548:g.543G>T
NG_009262.1:g.17551G>T , LRG_554:g.17551G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.740-72G>T MANE Select ENSP00000329546.4:n.740-72G>T
ENST00000346342.7:c.740-72G>T ENSP00000329546.3:n.740-72G>T
ENST00000375581.3:c.806-72G>T ENSP00000364731.3:n.806-72G>T
ENST00000541084.5:c.554-72G>T ENSP00000442051.2:n.554-72G>T
NM_000131.4:c.806-72G>T , LRG_554t1:c.806-72G>T NP_000122.1:n.806-72G>T
NM_001267554.1:c.554-72G>T NP_001254483.1:n.554-72G>T
NM_019616.3:c.740-72G>T , LRG_554t2:c.740-72G>T NP_062562.1:n.740-72G>T
NR_051961.1:n.827-72G>T
XM_006719963.2:c.599-72G>T XP_006720026.1:n.599-72G>T
XM_011537474.1:c.848-72G>T XP_011535776.1:n.848-72G>T
XM_011537475.1:c.662-72G>T XP_011535777.1:n.662-72G>T
XM_011537476.1:c.500-72G>T XP_011535778.1:n.500-72G>T
XM_011537477.1:c.809-72G>T XP_011535779.1:n.809-72G>T
XM_006719963.3:c.644-72G>T XP_006720026.2:n.644-72G>T
XM_011537474.2:c.893-72G>T XP_011535776.2:n.893-72G>T
XM_011537475.2:c.707-72G>T XP_011535777.2:n.707-72G>T
XM_011537476.2:c.500-72G>T XP_011535778.1:n.500-72G>T
NM_019616.4:c.740-72G>T MANE Select NP_062562.1:n.740-72G>T
NR_051961.2:n.824-72G>T
NM_001267554.2:c.554-72G>T NP_001254483.1:n.554-72G>T