Canonical Allele Identifier: CA388786004

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772849C>A (hg19) ; chr13:g.113118535C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118535C>A , CM000675.2:g.113118535C>A	GRCh38
NC_000013.10:g.113772849C>A , CM000675.1:g.113772849C>A	GRCh37
NC_000013.9:g.112820850C>A	NCBI36
NG_009258.1:g.737C>A , LRG_548:g.737C>A
NG_009262.1:g.17745C>A , LRG_554:g.17745C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.862C>A MANE Select	ENSP00000329546.4:p.Gln288Lys
ENST00000346342.7:c.862C>A	ENSP00000329546.3:p.Gln288Lys
ENST00000375581.3:c.928C>A	ENSP00000364731.3:p.Gln310Lys
ENST00000541084.5:c.676C>A	ENSP00000442051.2:p.Gln226Lys
NM_000131.4:c.928C>A , LRG_554t1:c.928C>A	NP_000122.1:p.Gln310Lys
NM_001267554.1:c.676C>A	NP_001254483.1:p.Gln226Lys
NM_019616.3:c.862C>A , LRG_554t2:c.862C>A	NP_062562.1:p.Gln288Lys
NR_051961.1:n.949C>A
XM_006719963.2:c.721C>A	XP_006720026.1:p.Gln241Lys
XM_011537474.1:c.970C>A	XP_011535776.1:p.Gln324Lys
XM_011537475.1:c.784C>A	XP_011535777.1:p.Gln262Lys
XM_011537476.1:c.622C>A	XP_011535778.1:p.Gln208Lys
XM_011537477.1:c.931C>A	XP_011535779.1:p.Gln311Lys
XM_006719963.3:c.766C>A	XP_006720026.2:p.Gln256Lys
XM_011537474.2:c.1015C>A	XP_011535776.2:p.Gln339Lys
XM_011537475.2:c.829C>A	XP_011535777.2:p.Gln277Lys
XM_011537476.2:c.622C>A	XP_011535778.1:p.Gln208Lys
NM_019616.4:c.862C>A MANE Select	NP_062562.1:p.Gln288Lys
NR_051961.2:n.946C>A
NM_001267554.2:c.676C>A	NP_001254483.1:p.Gln226Lys