Canonical Allele Identifier: CA388787220

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773309C>G (hg19) ; chr13:g.113118995C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118995C>G , CM000675.2:g.113118995C>G	GRCh38
NC_000013.10:g.113773309C>G , CM000675.1:g.113773309C>G	GRCh37
NC_000013.9:g.112821310C>G	NCBI36
NG_009258.1:g.1197C>G , LRG_548:g.1197C>G
NG_009262.1:g.18205C>G , LRG_554:g.18205C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1322C>G MANE Select	ENSP00000329546.4:p.Ala441Gly
ENST00000346342.7:c.1322C>G	ENSP00000329546.3:p.Ala441Gly
ENST00000375581.3:c.1388C>G	ENSP00000364731.3:p.Ala463Gly
ENST00000541084.5:c.1136C>G	ENSP00000442051.2:p.Ala379Gly
NM_000131.4:c.1388C>G , LRG_554t1:c.1388C>G	NP_000122.1:p.Ala463Gly
NM_001267554.1:c.1136C>G	NP_001254483.1:p.Ala379Gly
NM_019616.3:c.1322C>G , LRG_554t2:c.1322C>G	NP_062562.1:p.Ala441Gly
NR_051961.1:n.1409C>G
XM_006719963.2:c.1181C>G	XP_006720026.1:p.Ala394Gly
XM_011537474.1:c.1430C>G	XP_011535776.1:p.Ala477Gly
XM_011537475.1:c.1244C>G	XP_011535777.1:p.Ala415Gly
XM_011537476.1:c.1082C>G	XP_011535778.1:p.Ala361Gly
XM_011537477.1:c.1391C>G	XP_011535779.1:p.Ala464Gly
XM_006719963.3:c.1226C>G	XP_006720026.2:p.Ala409Gly
XM_011537474.2:c.1475C>G	XP_011535776.2:p.Ala492Gly
XM_011537475.2:c.1289C>G	XP_011535777.2:p.Ala430Gly
XM_011537476.2:c.1082C>G	XP_011535778.1:p.Ala361Gly
NM_019616.4:c.1322C>G MANE Select	NP_062562.1:p.Ala441Gly
NR_051961.2:n.1406C>G
NM_001267554.2:c.1136C>G	NP_001254483.1:p.Ala379Gly