Canonical Allele Identifier: CA485423991

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773001C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118687C>T , CM000675.2:g.113118687C>T	GRCh38
NC_000013.10:g.113773001C>T , CM000675.1:g.113773001C>T	GRCh37
NC_000013.9:g.112821002C>T	NCBI36
NG_009258.1:g.889C>T , LRG_548:g.889C>T
NG_009262.1:g.17897C>T , LRG_554:g.17897C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1014C>T MANE Select	ENSP00000329546.4:p.Leu338=
ENST00000346342.7:c.1014C>T	ENSP00000329546.3:p.Leu338=
ENST00000375581.3:c.1080C>T	ENSP00000364731.3:p.Leu360=
ENST00000541084.5:c.828C>T	ENSP00000442051.2:p.Leu276=
NM_000131.4:c.1080C>T , LRG_554t1:c.1080C>T	NP_000122.1:p.Leu360=
NM_001267554.1:c.828C>T	NP_001254483.1:p.Leu276=
NM_019616.3:c.1014C>T , LRG_554t2:c.1014C>T	NP_062562.1:p.Leu338=
NR_051961.1:n.1101C>T
XM_006719963.2:c.873C>T	XP_006720026.1:p.Leu291=
XM_011537474.1:c.1122C>T	XP_011535776.1:p.Leu374=
XM_011537475.1:c.936C>T	XP_011535777.1:p.Leu312=
XM_011537476.1:c.774C>T	XP_011535778.1:p.Leu258=
XM_011537477.1:c.1083C>T	XP_011535779.1:p.Leu361=
XM_006719963.3:c.918C>T	XP_006720026.2:p.Leu306=
XM_011537474.2:c.1167C>T	XP_011535776.2:p.Leu389=
XM_011537475.2:c.981C>T	XP_011535777.2:p.Leu327=
XM_011537476.2:c.774C>T	XP_011535778.1:p.Leu258=
NM_019616.4:c.1014C>T MANE Select	NP_062562.1:p.Leu338=
NR_051961.2:n.1098C>T
NM_001267554.2:c.828C>T	NP_001254483.1:p.Leu276=