Canonical Allele Identifier: CA485424001

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773014C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118700C>T , CM000675.2:g.113118700C>T	GRCh38
NC_000013.10:g.113773014C>T , CM000675.1:g.113773014C>T	GRCh37
NC_000013.9:g.112821015C>T	NCBI36
NG_009258.1:g.902C>T , LRG_548:g.902C>T
NG_009262.1:g.17910C>T , LRG_554:g.17910C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1027C>T MANE Select	ENSP00000329546.4:p.Leu343=
ENST00000346342.7:c.1027C>T	ENSP00000329546.3:p.Leu343=
ENST00000375581.3:c.1093C>T	ENSP00000364731.3:p.Leu365=
ENST00000541084.5:c.841C>T	ENSP00000442051.2:p.Leu281=
NM_000131.4:c.1093C>T , LRG_554t1:c.1093C>T	NP_000122.1:p.Leu365=
NM_001267554.1:c.841C>T	NP_001254483.1:p.Leu281=
NM_019616.3:c.1027C>T , LRG_554t2:c.1027C>T	NP_062562.1:p.Leu343=
NR_051961.1:n.1114C>T
XM_006719963.2:c.886C>T	XP_006720026.1:p.Leu296=
XM_011537474.1:c.1135C>T	XP_011535776.1:p.Leu379=
XM_011537475.1:c.949C>T	XP_011535777.1:p.Leu317=
XM_011537476.1:c.787C>T	XP_011535778.1:p.Leu263=
XM_011537477.1:c.1096C>T	XP_011535779.1:p.Leu366=
XM_006719963.3:c.931C>T	XP_006720026.2:p.Leu311=
XM_011537474.2:c.1180C>T	XP_011535776.2:p.Leu394=
XM_011537475.2:c.994C>T	XP_011535777.2:p.Leu332=
XM_011537476.2:c.787C>T	XP_011535778.1:p.Leu263=
NM_019616.4:c.1027C>T MANE Select	NP_062562.1:p.Leu343=
NR_051961.2:n.1111C>T
NM_001267554.2:c.841C>T	NP_001254483.1:p.Leu281=