Canonical Allele Identifier: CA7060228

Gene: F7

Linked Data

• dbSNP Id: rs373135581
• ExAC: 13:113773065 A / G
• gnomAD v2: 13-113773065-A-G
• gnomAD v3: 13-113118751-A-G
• gnomAD v4: 13-113118751-A-G
• MyVariant Identifiers: chr13:g.113773065A>G (hg19) ; chr13:g.113118751A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118751A>G , CM000675.2:g.113118751A>G	GRCh38
NC_000013.10:g.113773065A>G , CM000675.1:g.113773065A>G	GRCh37
NC_000013.9:g.112821066A>G	NCBI36
NG_009258.1:g.953A>G , LRG_548:g.953A>G
NG_009262.1:g.17961A>G , LRG_554:g.17961A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1078A>G MANE Select	ENSP00000329546.4:p.Asn360Asp
ENST00000346342.7:c.1078A>G	ENSP00000329546.3:p.Asn360Asp
ENST00000375581.3:c.1144A>G	ENSP00000364731.3:p.Asn382Asp
ENST00000541084.5:c.892A>G	ENSP00000442051.2:p.Asn298Asp
NM_000131.4:c.1144A>G , LRG_554t1:c.1144A>G	NP_000122.1:p.Asn382Asp
NM_001267554.1:c.892A>G	NP_001254483.1:p.Asn298Asp
NM_019616.3:c.1078A>G , LRG_554t2:c.1078A>G	NP_062562.1:p.Asn360Asp
NR_051961.1:n.1165A>G
XM_006719963.2:c.937A>G	XP_006720026.1:p.Asn313Asp
XM_011537474.1:c.1186A>G	XP_011535776.1:p.Asn396Asp
XM_011537475.1:c.1000A>G	XP_011535777.1:p.Asn334Asp
XM_011537476.1:c.838A>G	XP_011535778.1:p.Asn280Asp
XM_011537477.1:c.1147A>G	XP_011535779.1:p.Asn383Asp
XM_006719963.3:c.982A>G	XP_006720026.2:p.Asn328Asp
XM_011537474.2:c.1231A>G	XP_011535776.2:p.Asn411Asp
XM_011537475.2:c.1045A>G	XP_011535777.2:p.Asn349Asp
XM_011537476.2:c.838A>G	XP_011535778.1:p.Asn280Asp
NM_019616.4:c.1078A>G MANE Select	NP_062562.1:p.Asn360Asp
NR_051961.2:n.1162A>G
NM_001267554.2:c.892A>G	NP_001254483.1:p.Asn298Asp