Canonical Allele Identifier: CA388780720

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113110711C>G , CM000675.2:g.113110711C>G	GRCh38
NC_000013.10:g.113765025C>G , CM000675.1:g.113765025C>G	GRCh37
NC_000013.9:g.112813026C>G	NCBI36
NG_009262.1:g.9921C>G , LRG_554:g.9921C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.86C>G MANE Select	NP_062562.1:p.Ala29Gly
ENST00000346342.8:c.86C>G MANE Select	ENSP00000329546.4:p.Ala29Gly
NM_000131.4:c.152C>G , LRG_554t1:c.152C>G	NP_000122.1:p.Ala51Gly
NM_001267554.1:c.65-3136C>G	NP_001254483.1:n.65-3136C>G
NM_001267554.2:c.65-3136C>G	NP_001254483.1:n.65-3136C>G
NM_019616.3:c.86C>G , LRG_554t2:c.86C>G	NP_062562.1:p.Ala29Gly
NR_051961.1:n.126C>G
NR_051961.2:n.123C>G
ENST00000346342.7:c.86C>G	ENSP00000329546.3:p.Ala29Gly
ENST00000375581.3:c.152C>G	ENSP00000364731.3:p.Ala51Gly
ENST00000444337.1:c.72C>G	ENSP00000387669.1:p.Ser24Arg
ENST00000473085.1:n.33C>G
ENST00000479674.1:n.372C>G
ENST00000541084.5:c.65-3136C>G	ENSP00000442051.2:n.65-3136C>G
XM_006719963.2:c.86C>G	XP_006720026.1:p.Ala29Gly
XM_006719963.3:c.131C>G	XP_006720026.2:p.Ala44Gly
XM_011537474.1:c.86C>G	XP_011535776.1:p.Ala29Gly
XM_011537474.2:c.131C>G	XP_011535776.2:p.Ala44Gly
XM_011537475.1:c.65-3136C>G	XP_011535777.1:n.65-3136C>G
XM_011537475.2:c.110-3136C>G	XP_011535777.2:n.110-3136C>G
XM_011537477.1:c.72C>G	XP_011535779.1:p.Ser24Arg