Canonical Allele Identifier: CA388782342

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768226T>A (hg19) ; chr13:g.113113912T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113912T>A , CM000675.2:g.113113912T>A	GRCh38
NC_000013.10:g.113768226T>A , CM000675.1:g.113768226T>A	GRCh37
NC_000013.9:g.112816227T>A	NCBI36
NG_009262.1:g.13122T>A , LRG_554:g.13122T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.316T>A MANE Select	ENSP00000329546.4:p.Tyr106Asn
ENST00000346342.7:c.316T>A	ENSP00000329546.3:p.Tyr106Asn
ENST00000375581.3:c.382T>A	ENSP00000364731.3:p.Tyr128Asn
ENST00000444337.1:c.*124T>A	ENSP00000387669.1:n.*124T>A
ENST00000473085.1:n.263T>A
ENST00000479674.1:n.649T>A
ENST00000541084.5:c.130T>A	ENSP00000442051.2:p.Tyr44Asn
NM_000131.4:c.382T>A , LRG_554t1:c.382T>A	NP_000122.1:p.Tyr128Asn
NM_001267554.1:c.130T>A	NP_001254483.1:p.Tyr44Asn
NM_019616.3:c.316T>A , LRG_554t2:c.316T>A	NP_062562.1:p.Tyr106Asn
NR_051961.1:n.403T>A
XM_006719963.2:c.316T>A	XP_006720026.1:p.Tyr106Asn
XM_011537474.1:c.316T>A	XP_011535776.1:p.Tyr106Asn
XM_011537475.1:c.130T>A	XP_011535777.1:p.Tyr44Asn
XM_011537477.1:c.277T>A	XP_011535779.1:p.Tyr93Asn
XM_006719963.3:c.361T>A	XP_006720026.2:p.Tyr121Asn
XM_011537474.2:c.361T>A	XP_011535776.2:p.Tyr121Asn
XM_011537475.2:c.175T>A	XP_011535777.2:p.Tyr59Asn
NM_019616.4:c.316T>A MANE Select	NP_062562.1:p.Tyr106Asn
NR_051961.2:n.400T>A
NM_001267554.2:c.130T>A	NP_001254483.1:p.Tyr44Asn