Canonical Allele Identifier: CA388786178

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772939T>G (hg19) ; chr13:g.113118625T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118625T>G , CM000675.2:g.113118625T>G	GRCh38
NC_000013.10:g.113772939T>G , CM000675.1:g.113772939T>G	GRCh37
NC_000013.9:g.112820940T>G	NCBI36
NG_009258.1:g.827T>G , LRG_548:g.827T>G
NG_009262.1:g.17835T>G , LRG_554:g.17835T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.952T>G MANE Select	ENSP00000329546.4:p.Leu318Val
ENST00000346342.7:c.952T>G	ENSP00000329546.3:p.Leu318Val
ENST00000375581.3:c.1018T>G	ENSP00000364731.3:p.Leu340Val
ENST00000541084.5:c.766T>G	ENSP00000442051.2:p.Leu256Val
NM_000131.4:c.1018T>G , LRG_554t1:c.1018T>G	NP_000122.1:p.Leu340Val
NM_001267554.1:c.766T>G	NP_001254483.1:p.Leu256Val
NM_019616.3:c.952T>G , LRG_554t2:c.952T>G	NP_062562.1:p.Leu318Val
NR_051961.1:n.1039T>G
XM_006719963.2:c.811T>G	XP_006720026.1:p.Leu271Val
XM_011537474.1:c.1060T>G	XP_011535776.1:p.Leu354Val
XM_011537475.1:c.874T>G	XP_011535777.1:p.Leu292Val
XM_011537476.1:c.712T>G	XP_011535778.1:p.Leu238Val
XM_011537477.1:c.1021T>G	XP_011535779.1:p.Leu341Val
XM_006719963.3:c.856T>G	XP_006720026.2:p.Leu286Val
XM_011537474.2:c.1105T>G	XP_011535776.2:p.Leu369Val
XM_011537475.2:c.919T>G	XP_011535777.2:p.Leu307Val
XM_011537476.2:c.712T>G	XP_011535778.1:p.Leu238Val
NM_019616.4:c.952T>G MANE Select	NP_062562.1:p.Leu318Val
NR_051961.2:n.1036T>G
NM_001267554.2:c.766T>G	NP_001254483.1:p.Leu256Val