Canonical Allele Identifier: CA7060089

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113117601G>A , CM000675.2:g.113117601G>A	GRCh38
NC_000013.10:g.113771915G>A , CM000675.1:g.113771915G>A	GRCh37
NC_000013.9:g.112819916G>A	NCBI36
NG_009262.1:g.16811G>A , LRG_554:g.16811G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.739+5G>A MANE Select	NP_062562.1:n.739+5G>A
ENST00000346342.8:c.739+5G>A MANE Select	ENSP00000329546.4:n.739+5G>A
NM_000131.4:c.805+5G>A , LRG_554t1:c.805+5G>A	NP_000122.1:n.805+5G>A
NM_001267554.1:c.553+5G>A	NP_001254483.1:n.553+5G>A
NM_001267554.2:c.553+5G>A	NP_001254483.1:n.553+5G>A
NM_019616.3:c.739+5G>A , LRG_554t2:c.739+5G>A	NP_062562.1:n.739+5G>A
NR_051961.1:n.826+5G>A
NR_051961.2:n.823+5G>A
ENST00000346342.7:c.739+5G>A	ENSP00000329546.3:n.739+5G>A
ENST00000375581.3:c.805+5G>A	ENSP00000364731.3:n.805+5G>A
ENST00000541084.5:c.553+5G>A	ENSP00000442051.2:n.553+5G>A
XM_006719963.2:c.598+5G>A	XP_006720026.1:n.598+5G>A
XM_006719963.3:c.643+5G>A	XP_006720026.2:n.643+5G>A
XM_011537474.1:c.847+5G>A	XP_011535776.1:n.847+5G>A
XM_011537474.2:c.892+5G>A	XP_011535776.2:n.892+5G>A
XM_011537475.1:c.661+5G>A	XP_011535777.1:n.661+5G>A
XM_011537475.2:c.706+5G>A	XP_011535777.2:n.706+5G>A
XM_011537476.1:c.499+5G>A	XP_011535778.1:n.499+5G>A
XM_011537476.2:c.499+5G>A	XP_011535778.1:n.499+5G>A
XM_011537477.1:c.808+5G>A	XP_011535779.1:n.808+5G>A