Canonical Allele Identifier: CA7060261
Gene: F7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113118940G>A , CM000675.2:g.113118940G>A GRCh38
NC_000013.10:g.113773254G>A , CM000675.1:g.113773254G>A GRCh37
NC_000013.9:g.112821255G>A NCBI36
NG_009258.1:g.1142G>A , LRG_548:g.1142G>A
NG_009262.1:g.18150G>A , LRG_554:g.18150G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000346342.8:c.1267G>A MANE Select ENSP00000329546.4:p.Glu423Lys
ENST00000346342.7:c.1267G>A ENSP00000329546.3:p.Glu423Lys
ENST00000375581.3:c.1333G>A ENSP00000364731.3:p.Glu445Lys
ENST00000541084.5:c.1081G>A ENSP00000442051.2:p.Glu361Lys
NM_000131.4:c.1333G>A , LRG_554t1:c.1333G>A NP_000122.1:p.Glu445Lys
NM_001267554.1:c.1081G>A NP_001254483.1:p.Glu361Lys
NM_019616.3:c.1267G>A , LRG_554t2:c.1267G>A NP_062562.1:p.Glu423Lys
NR_051961.1:n.1354G>A
XM_006719963.2:c.1126G>A XP_006720026.1:p.Glu376Lys
XM_011537474.1:c.1375G>A XP_011535776.1:p.Glu459Lys
XM_011537475.1:c.1189G>A XP_011535777.1:p.Glu397Lys
XM_011537476.1:c.1027G>A XP_011535778.1:p.Glu343Lys
XM_011537477.1:c.1336G>A XP_011535779.1:p.Glu446Lys
XM_006719963.3:c.1171G>A XP_006720026.2:p.Glu391Lys
XM_011537474.2:c.1420G>A XP_011535776.2:p.Glu474Lys
XM_011537475.2:c.1234G>A XP_011535777.2:p.Glu412Lys
XM_011537476.2:c.1027G>A XP_011535778.1:p.Glu343Lys
NM_019616.4:c.1267G>A MANE Select NP_062562.1:p.Glu423Lys
NR_051961.2:n.1351G>A
NM_001267554.2:c.1081G>A NP_001254483.1:p.Glu361Lys