Canonical Allele Identifier: CA485423873

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772834C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118520C>T , CM000675.2:g.113118520C>T	GRCh38
NC_000013.10:g.113772834C>T , CM000675.1:g.113772834C>T	GRCh37
NC_000013.9:g.112820835C>T	NCBI36
NG_009258.1:g.722C>T , LRG_548:g.722C>T
NG_009262.1:g.17730C>T , LRG_554:g.17730C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.847C>T MANE Select	ENSP00000329546.4:p.Leu283=
ENST00000346342.7:c.847C>T	ENSP00000329546.3:p.Leu283=
ENST00000375581.3:c.913C>T	ENSP00000364731.3:p.Leu305=
ENST00000541084.5:c.661C>T	ENSP00000442051.2:p.Leu221=
NM_000131.4:c.913C>T , LRG_554t1:c.913C>T	NP_000122.1:p.Leu305=
NM_001267554.1:c.661C>T	NP_001254483.1:p.Leu221=
NM_019616.3:c.847C>T , LRG_554t2:c.847C>T	NP_062562.1:p.Leu283=
NR_051961.1:n.934C>T
XM_006719963.2:c.706C>T	XP_006720026.1:p.Leu236=
XM_011537474.1:c.955C>T	XP_011535776.1:p.Leu319=
XM_011537475.1:c.769C>T	XP_011535777.1:p.Leu257=
XM_011537476.1:c.607C>T	XP_011535778.1:p.Leu203=
XM_011537477.1:c.916C>T	XP_011535779.1:p.Leu306=
XM_006719963.3:c.751C>T	XP_006720026.2:p.Leu251=
XM_011537474.2:c.1000C>T	XP_011535776.2:p.Leu334=
XM_011537475.2:c.814C>T	XP_011535777.2:p.Leu272=
XM_011537476.2:c.607C>T	XP_011535778.1:p.Leu203=
NM_019616.4:c.847C>T MANE Select	NP_062562.1:p.Leu283=
NR_051961.2:n.931C>T
NM_001267554.2:c.661C>T	NP_001254483.1:p.Leu221=