Canonical Allele Identifier: CA388786155

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772926C>G (hg19) ; chr13:g.113118612C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118612C>G , CM000675.2:g.113118612C>G	GRCh38
NC_000013.10:g.113772926C>G , CM000675.1:g.113772926C>G	GRCh37
NC_000013.9:g.112820927C>G	NCBI36
NG_009258.1:g.814C>G , LRG_548:g.814C>G
NG_009262.1:g.17822C>G , LRG_554:g.17822C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.939C>G MANE Select	ENSP00000329546.4:p.Phe313Leu
ENST00000346342.7:c.939C>G	ENSP00000329546.3:p.Phe313Leu
ENST00000375581.3:c.1005C>G	ENSP00000364731.3:p.Phe335Leu
ENST00000541084.5:c.753C>G	ENSP00000442051.2:p.Phe251Leu
NM_000131.4:c.1005C>G , LRG_554t1:c.1005C>G	NP_000122.1:p.Phe335Leu
NM_001267554.1:c.753C>G	NP_001254483.1:p.Phe251Leu
NM_019616.3:c.939C>G , LRG_554t2:c.939C>G	NP_062562.1:p.Phe313Leu
NR_051961.1:n.1026C>G
XM_006719963.2:c.798C>G	XP_006720026.1:p.Phe266Leu
XM_011537474.1:c.1047C>G	XP_011535776.1:p.Phe349Leu
XM_011537475.1:c.861C>G	XP_011535777.1:p.Phe287Leu
XM_011537476.1:c.699C>G	XP_011535778.1:p.Phe233Leu
XM_011537477.1:c.1008C>G	XP_011535779.1:p.Phe336Leu
XM_006719963.3:c.843C>G	XP_006720026.2:p.Phe281Leu
XM_011537474.2:c.1092C>G	XP_011535776.2:p.Phe364Leu
XM_011537475.2:c.906C>G	XP_011535777.2:p.Phe302Leu
XM_011537476.2:c.699C>G	XP_011535778.1:p.Phe233Leu
NM_019616.4:c.939C>G MANE Select	NP_062562.1:p.Phe313Leu
NR_051961.2:n.1023C>G
NM_001267554.2:c.753C>G	NP_001254483.1:p.Phe251Leu