Canonical Allele Identifier: CA2120144809
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113119853T= , CM000675.2:g.113119853T= GRCh38
NC_000013.10:g.113774167T= , CM000675.1:g.113774167T= GRCh37
NC_000013.9:g.112822168T= NCBI36
NG_009258.1:g.2055T= , LRG_548:g.2055T=
NG_009262.1:g.19063T= , LRG_554:g.19063T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.*845T= MANE Select ENSP00000329546.4:n.*845T=
ENST00000346342.7:c.*845T= ENSP00000329546.3:n.*845T=
ENST00000375581.3:c.*845T= ENSP00000364731.3:n.*845T=
ENST00000541084.5:c.*845T= ENSP00000442051.2:n.*845T=
NM_000131.4:c.*845T= , LRG_554t1:c.*845T= NP_000122.1:n.*845T=
NM_001267554.1:c.*845T= NP_001254483.1:n.*845T=
NM_019616.3:c.*845T= , LRG_554t2:c.*845T= NP_062562.1:n.*845T=
NR_051961.1:n.2267T=
XM_006719963.2:c.*845T= XP_006720026.1:n.*845T=
XM_011537474.1:c.*845T= XP_011535776.1:n.*845T=
XM_011537475.1:c.*845T= XP_011535777.1:n.*845T=
XM_011537476.1:c.*845T= XP_011535778.1:n.*845T=
XM_011537477.1:c.*845T= XP_011535779.1:n.*845T=
XM_006719963.3:c.*845T= XP_006720026.2:n.*845T=
XM_011537474.2:c.*845T= XP_011535776.2:n.*845T=
XM_011537475.2:c.*845T= XP_011535777.2:n.*845T=
XM_011537476.2:c.*845T= XP_011535778.1:n.*845T=
NM_019616.4:c.*845T= MANE Select NP_062562.1:n.*845T=
NR_051961.2:n.2264T=
NM_001267554.2:c.*845T= NP_001254483.1:n.*845T=