Canonical Allele Identifier: CA388785951

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772821C>G (hg19) ; chr13:g.113118507C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118507C>G , CM000675.2:g.113118507C>G	GRCh38
NC_000013.10:g.113772821C>G , CM000675.1:g.113772821C>G	GRCh37
NC_000013.9:g.112820822C>G	NCBI36
NG_009258.1:g.709C>G , LRG_548:g.709C>G
NG_009262.1:g.17717C>G , LRG_554:g.17717C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.834C>G MANE Select	ENSP00000329546.4:p.Asn278Lys
ENST00000346342.7:c.834C>G	ENSP00000329546.3:p.Asn278Lys
ENST00000375581.3:c.900C>G	ENSP00000364731.3:p.Asn300Lys
ENST00000541084.5:c.648C>G	ENSP00000442051.2:p.Asn216Lys
NM_000131.4:c.900C>G , LRG_554t1:c.900C>G	NP_000122.1:p.Asn300Lys
NM_001267554.1:c.648C>G	NP_001254483.1:p.Asn216Lys
NM_019616.3:c.834C>G , LRG_554t2:c.834C>G	NP_062562.1:p.Asn278Lys
NR_051961.1:n.921C>G
XM_006719963.2:c.693C>G	XP_006720026.1:p.Asn231Lys
XM_011537474.1:c.942C>G	XP_011535776.1:p.Asn314Lys
XM_011537475.1:c.756C>G	XP_011535777.1:p.Asn252Lys
XM_011537476.1:c.594C>G	XP_011535778.1:p.Asn198Lys
XM_011537477.1:c.903C>G	XP_011535779.1:p.Asn301Lys
XM_006719963.3:c.738C>G	XP_006720026.2:p.Asn246Lys
XM_011537474.2:c.987C>G	XP_011535776.2:p.Asn329Lys
XM_011537475.2:c.801C>G	XP_011535777.2:p.Asn267Lys
XM_011537476.2:c.594C>G	XP_011535778.1:p.Asn198Lys
NM_019616.4:c.834C>G MANE Select	NP_062562.1:p.Asn278Lys
NR_051961.2:n.918C>G
NM_001267554.2:c.648C>G	NP_001254483.1:p.Asn216Lys