Canonical Allele Identifier: CA388782347
Gene: F7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113113913A>C , CM000675.2:g.113113913A>C GRCh38
NC_000013.10:g.113768227A>C , CM000675.1:g.113768227A>C GRCh37
NC_000013.9:g.112816228A>C NCBI36
NG_009262.1:g.13123A>C , LRG_554:g.13123A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.317A>C MANE Select ENSP00000329546.4:p.Tyr106Ser
ENST00000346342.7:c.317A>C ENSP00000329546.3:p.Tyr106Ser
ENST00000375581.3:c.383A>C ENSP00000364731.3:p.Tyr128Ser
ENST00000444337.1:c.*125A>C ENSP00000387669.1:n.*125A>C
ENST00000473085.1:n.264A>C
ENST00000479674.1:n.650A>C
ENST00000541084.5:c.131A>C ENSP00000442051.2:p.Tyr44Ser
NM_000131.4:c.383A>C , LRG_554t1:c.383A>C NP_000122.1:p.Tyr128Ser
NM_001267554.1:c.131A>C NP_001254483.1:p.Tyr44Ser
NM_019616.3:c.317A>C , LRG_554t2:c.317A>C NP_062562.1:p.Tyr106Ser
NR_051961.1:n.404A>C
XM_006719963.2:c.317A>C XP_006720026.1:p.Tyr106Ser
XM_011537474.1:c.317A>C XP_011535776.1:p.Tyr106Ser
XM_011537475.1:c.131A>C XP_011535777.1:p.Tyr44Ser
XM_011537477.1:c.278A>C XP_011535779.1:p.Tyr93Ser
XM_006719963.3:c.362A>C XP_006720026.2:p.Tyr121Ser
XM_011537474.2:c.362A>C XP_011535776.2:p.Tyr121Ser
XM_011537475.2:c.176A>C XP_011535777.2:p.Tyr59Ser
NM_019616.4:c.317A>C MANE Select NP_062562.1:p.Tyr106Ser
NR_051961.2:n.401A>C
NM_001267554.2:c.131A>C NP_001254483.1:p.Tyr44Ser