Canonical Allele Identifier: CA485423824

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772755G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118441G>C , CM000675.2:g.113118441G>C	GRCh38
NC_000013.10:g.113772755G>C , CM000675.1:g.113772755G>C	GRCh37
NC_000013.9:g.112820756G>C	NCBI36
NG_009258.1:g.643G>C , LRG_548:g.643G>C
NG_009262.1:g.17651G>C , LRG_554:g.17651G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.768G>C MANE Select	ENSP00000329546.4:p.Gly256=
ENST00000346342.7:c.768G>C	ENSP00000329546.3:p.Gly256=
ENST00000375581.3:c.834G>C	ENSP00000364731.3:p.Gly278=
ENST00000541084.5:c.582G>C	ENSP00000442051.2:p.Gly194=
NM_000131.4:c.834G>C , LRG_554t1:c.834G>C	NP_000122.1:p.Gly278=
NM_001267554.1:c.582G>C	NP_001254483.1:p.Gly194=
NM_019616.3:c.768G>C , LRG_554t2:c.768G>C	NP_062562.1:p.Gly256=
NR_051961.1:n.855G>C
XM_006719963.2:c.627G>C	XP_006720026.1:p.Gly209=
XM_011537474.1:c.876G>C	XP_011535776.1:p.Gly292=
XM_011537475.1:c.690G>C	XP_011535777.1:p.Gly230=
XM_011537476.1:c.528G>C	XP_011535778.1:p.Gly176=
XM_011537477.1:c.837G>C	XP_011535779.1:p.Gly279=
XM_006719963.3:c.672G>C	XP_006720026.2:p.Gly224=
XM_011537474.2:c.921G>C	XP_011535776.2:p.Gly307=
XM_011537475.2:c.735G>C	XP_011535777.2:p.Gly245=
XM_011537476.2:c.528G>C	XP_011535778.1:p.Gly176=
NM_019616.4:c.768G>C MANE Select	NP_062562.1:p.Gly256=
NR_051961.2:n.852G>C
NM_001267554.2:c.582G>C	NP_001254483.1:p.Gly194=