Canonical Allele Identifier: CA2739291817
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113118812_113118824dup , CM000675.2:g.113118812_113118824dup GRCh38
NC_000013.10:g.113773126_113773138dup , CM000675.1:g.113773126_113773138dup GRCh37
NC_000013.9:g.112821127_112821139dup NCBI36
NG_009258.1:g.1014_1026dup , LRG_548:g.1014_1026dup
NG_009262.1:g.18022_18034dup , LRG_554:g.18022_18034dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.1139_1151dup MANE Select ENSP00000329546.4:p.Pro385GlyfsTer?
ENST00000346342.7:c.1139_1151dup ENSP00000329546.3:p.Pro385GlyfsTer?
ENST00000375581.3:c.1205_1217dup ENSP00000364731.3:p.Pro407GlyfsTer?
ENST00000541084.5:c.953_965dup ENSP00000442051.2:p.Pro323GlyfsTer?
NM_000131.4:c.1205_1217dup , LRG_554t1:c.1205_1217dup NP_000122.1:p.Pro407GlyfsTer?
NM_001267554.1:c.953_965dup NP_001254483.1:p.Pro323GlyfsTer?
NM_019616.3:c.1139_1151dup , LRG_554t2:c.1139_1151dup NP_062562.1:p.Pro385GlyfsTer?
NR_051961.1:n.1226_1238dup
XM_006719963.2:c.998_1010dup XP_006720026.1:p.Pro338GlyfsTer?
XM_011537474.1:c.1247_1259dup XP_011535776.1:p.Pro421GlyfsTer?
XM_011537475.1:c.1061_1073dup XP_011535777.1:p.Pro359GlyfsTer?
XM_011537476.1:c.899_911dup XP_011535778.1:p.Pro305GlyfsTer?
XM_011537477.1:c.1208_1220dup XP_011535779.1:p.Pro408GlyfsTer?
XM_006719963.3:c.1043_1055dup XP_006720026.2:p.Pro353GlyfsTer?
XM_011537474.2:c.1292_1304dup XP_011535776.2:p.Pro436GlyfsTer?
XM_011537475.2:c.1106_1118dup XP_011535777.2:p.Pro374GlyfsTer?
XM_011537476.2:c.899_911dup XP_011535778.1:p.Pro305GlyfsTer?
NM_019616.4:c.1139_1151dup MANE Select NP_062562.1:p.Pro385GlyfsTer?
NR_051961.2:n.1223_1235dup
NM_001267554.2:c.953_965dup NP_001254483.1:p.Pro323GlyfsTer?