Canonical Allele Identifier: CA485423877

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772839C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118525C>A , CM000675.2:g.113118525C>A	GRCh38
NC_000013.10:g.113772839C>A , CM000675.1:g.113772839C>A	GRCh37
NC_000013.9:g.112820840C>A	NCBI36
NG_009258.1:g.727C>A , LRG_548:g.727C>A
NG_009262.1:g.17735C>A , LRG_554:g.17735C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.852C>A MANE Select	ENSP00000329546.4:p.Leu284=
ENST00000346342.7:c.852C>A	ENSP00000329546.3:p.Leu284=
ENST00000375581.3:c.918C>A	ENSP00000364731.3:p.Leu306=
ENST00000541084.5:c.666C>A	ENSP00000442051.2:p.Leu222=
NM_000131.4:c.918C>A , LRG_554t1:c.918C>A	NP_000122.1:p.Leu306=
NM_001267554.1:c.666C>A	NP_001254483.1:p.Leu222=
NM_019616.3:c.852C>A , LRG_554t2:c.852C>A	NP_062562.1:p.Leu284=
NR_051961.1:n.939C>A
XM_006719963.2:c.711C>A	XP_006720026.1:p.Leu237=
XM_011537474.1:c.960C>A	XP_011535776.1:p.Leu320=
XM_011537475.1:c.774C>A	XP_011535777.1:p.Leu258=
XM_011537476.1:c.612C>A	XP_011535778.1:p.Leu204=
XM_011537477.1:c.921C>A	XP_011535779.1:p.Leu307=
XM_006719963.3:c.756C>A	XP_006720026.2:p.Leu252=
XM_011537474.2:c.1005C>A	XP_011535776.2:p.Leu335=
XM_011537475.2:c.819C>A	XP_011535777.2:p.Leu273=
XM_011537476.2:c.612C>A	XP_011535778.1:p.Leu204=
NM_019616.4:c.852C>A MANE Select	NP_062562.1:p.Leu284=
NR_051961.2:n.936C>A
NM_001267554.2:c.666C>A	NP_001254483.1:p.Leu222=