Canonical Allele Identifier: CA388786160

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772928T>G (hg19) ; chr13:g.113118614T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118614T>G , CM000675.2:g.113118614T>G	GRCh38
NC_000013.10:g.113772928T>G , CM000675.1:g.113772928T>G	GRCh37
NC_000013.9:g.112820929T>G	NCBI36
NG_009258.1:g.816T>G , LRG_548:g.816T>G
NG_009262.1:g.17824T>G , LRG_554:g.17824T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.941T>G MANE Select	ENSP00000329546.4:p.Val314Gly
ENST00000346342.7:c.941T>G	ENSP00000329546.3:p.Val314Gly
ENST00000375581.3:c.1007T>G	ENSP00000364731.3:p.Val336Gly
ENST00000541084.5:c.755T>G	ENSP00000442051.2:p.Val252Gly
NM_000131.4:c.1007T>G , LRG_554t1:c.1007T>G	NP_000122.1:p.Val336Gly
NM_001267554.1:c.755T>G	NP_001254483.1:p.Val252Gly
NM_019616.3:c.941T>G , LRG_554t2:c.941T>G	NP_062562.1:p.Val314Gly
NR_051961.1:n.1028T>G
XM_006719963.2:c.800T>G	XP_006720026.1:p.Val267Gly
XM_011537474.1:c.1049T>G	XP_011535776.1:p.Val350Gly
XM_011537475.1:c.863T>G	XP_011535777.1:p.Val288Gly
XM_011537476.1:c.701T>G	XP_011535778.1:p.Val234Gly
XM_011537477.1:c.1010T>G	XP_011535779.1:p.Val337Gly
XM_006719963.3:c.845T>G	XP_006720026.2:p.Val282Gly
XM_011537474.2:c.1094T>G	XP_011535776.2:p.Val365Gly
XM_011537475.2:c.908T>G	XP_011535777.2:p.Val303Gly
XM_011537476.2:c.701T>G	XP_011535778.1:p.Val234Gly
NM_019616.4:c.941T>G MANE Select	NP_062562.1:p.Val314Gly
NR_051961.2:n.1025T>G
NM_001267554.2:c.755T>G	NP_001254483.1:p.Val252Gly