Canonical Allele Identifier: CA485423831

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772770G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118456G>C , CM000675.2:g.113118456G>C	GRCh38
NC_000013.10:g.113772770G>C , CM000675.1:g.113772770G>C	GRCh37
NC_000013.9:g.112820771G>C	NCBI36
NG_009258.1:g.658G>C , LRG_548:g.658G>C
NG_009262.1:g.17666G>C , LRG_554:g.17666G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.783G>C MANE Select	ENSP00000329546.4:p.Arg261=
ENST00000346342.7:c.783G>C	ENSP00000329546.3:p.Arg261=
ENST00000375581.3:c.849G>C	ENSP00000364731.3:p.Arg283=
ENST00000541084.5:c.597G>C	ENSP00000442051.2:p.Arg199=
NM_000131.4:c.849G>C , LRG_554t1:c.849G>C	NP_000122.1:p.Arg283=
NM_001267554.1:c.597G>C	NP_001254483.1:p.Arg199=
NM_019616.3:c.783G>C , LRG_554t2:c.783G>C	NP_062562.1:p.Arg261=
NR_051961.1:n.870G>C
XM_006719963.2:c.642G>C	XP_006720026.1:p.Arg214=
XM_011537474.1:c.891G>C	XP_011535776.1:p.Arg297=
XM_011537475.1:c.705G>C	XP_011535777.1:p.Arg235=
XM_011537476.1:c.543G>C	XP_011535778.1:p.Arg181=
XM_011537477.1:c.852G>C	XP_011535779.1:p.Arg284=
XM_006719963.3:c.687G>C	XP_006720026.2:p.Arg229=
XM_011537474.2:c.936G>C	XP_011535776.2:p.Arg312=
XM_011537475.2:c.750G>C	XP_011535777.2:p.Arg250=
XM_011537476.2:c.543G>C	XP_011535778.1:p.Arg181=
NM_019616.4:c.783G>C MANE Select	NP_062562.1:p.Arg261=
NR_051961.2:n.867G>C
NM_001267554.2:c.597G>C	NP_001254483.1:p.Arg199=