Canonical Allele Identifier: CA7060267

Gene: F7

Linked Data

• dbSNP Id: rs771423889
• ExAC: 13:113773283 G / A
• gnomAD v2: 13-113773283-G-A
• gnomAD v3: 13-113118969-G-A
• gnomAD v4: 13-113118969-G-A
• MyVariant Identifiers: chr13:g.113773283G>A (hg19) ; chr13:g.113118969G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118969G>A , CM000675.2:g.113118969G>A	GRCh38
NC_000013.10:g.113773283G>A , CM000675.1:g.113773283G>A	GRCh37
NC_000013.9:g.112821284G>A	NCBI36
NG_009258.1:g.1171G>A , LRG_548:g.1171G>A
NG_009262.1:g.18179G>A , LRG_554:g.18179G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1296G>A MANE Select	ENSP00000329546.4:p.Glu432=
ENST00000346342.7:c.1296G>A	ENSP00000329546.3:p.Glu432=
ENST00000375581.3:c.1362G>A	ENSP00000364731.3:p.Glu454=
ENST00000541084.5:c.1110G>A	ENSP00000442051.2:p.Glu370=
NM_000131.4:c.1362G>A , LRG_554t1:c.1362G>A	NP_000122.1:p.Glu454=
NM_001267554.1:c.1110G>A	NP_001254483.1:p.Glu370=
NM_019616.3:c.1296G>A , LRG_554t2:c.1296G>A	NP_062562.1:p.Glu432=
NR_051961.1:n.1383G>A
XM_006719963.2:c.1155G>A	XP_006720026.1:p.Glu385=
XM_011537474.1:c.1404G>A	XP_011535776.1:p.Glu468=
XM_011537475.1:c.1218G>A	XP_011535777.1:p.Glu406=
XM_011537476.1:c.1056G>A	XP_011535778.1:p.Glu352=
XM_011537477.1:c.1365G>A	XP_011535779.1:p.Glu455=
XM_006719963.3:c.1200G>A	XP_006720026.2:p.Glu400=
XM_011537474.2:c.1449G>A	XP_011535776.2:p.Glu483=
XM_011537475.2:c.1263G>A	XP_011535777.2:p.Glu421=
XM_011537476.2:c.1056G>A	XP_011535778.1:p.Glu352=
NM_019616.4:c.1296G>A MANE Select	NP_062562.1:p.Glu432=
NR_051961.2:n.1380G>A
NM_001267554.2:c.1110G>A	NP_001254483.1:p.Glu370=