Canonical Allele Identifier: CA2120145226
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113120069G= , CM000675.2:g.113120069G= GRCh38
NC_000013.10:g.113774383G= , CM000675.1:g.113774383G= GRCh37
NC_000013.9:g.112822384G= NCBI36
NG_009258.1:g.2271G= , LRG_548:g.2271G=
NG_009262.1:g.19279G= , LRG_554:g.19279G=

Transcript Alleles

HGVS Amino-acid change
ENST00000346342.8:c.*1061G= MANE Select ENSP00000329546.4:n.*1061G=
ENST00000375581.3:c.*1061G= ENSP00000364731.3:n.*1061G=
ENST00000541084.5:c.*1061G= ENSP00000442051.2:n.*1061G=
NM_000131.4:c.*1061G= , LRG_554t1:c.*1061G= NP_000122.1:n.*1061G=
NM_001267554.1:c.*1061G= NP_001254483.1:n.*1061G=
NM_019616.3:c.*1061G= , LRG_554t2:c.*1061G= NP_062562.1:n.*1061G=
NR_051961.1:n.2483G=
XM_006719963.2:c.*1061G= XP_006720026.1:n.*1061G=
XM_011537474.1:c.*1061G= XP_011535776.1:n.*1061G=
XM_011537475.1:c.*1061G= XP_011535777.1:n.*1061G=
XM_011537476.1:c.*1061G= XP_011535778.1:n.*1061G=
XM_011537477.1:c.*1061G= XP_011535779.1:n.*1061G=
XM_006719963.3:c.*1061G= XP_006720026.2:n.*1061G=
XM_011537474.2:c.*1061G= XP_011535776.2:n.*1061G=
XM_011537475.2:c.*1061G= XP_011535777.2:n.*1061G=
XM_011537476.2:c.*1061G= XP_011535778.1:n.*1061G=
NM_019616.4:c.*1061G= MANE Select NP_062562.1:n.*1061G=
NR_051961.2:n.2480G=
NM_001267554.2:c.*1061G= NP_001254483.1:n.*1061G=