Canonical Allele Identifier: CA388785841

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772763A>C (hg19) ; chr13:g.113118449A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118449A>C , CM000675.2:g.113118449A>C	GRCh38
NC_000013.10:g.113772763A>C , CM000675.1:g.113772763A>C	GRCh37
NC_000013.9:g.112820764A>C	NCBI36
NG_009258.1:g.651A>C , LRG_548:g.651A>C
NG_009262.1:g.17659A>C , LRG_554:g.17659A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.776A>C MANE Select	ENSP00000329546.4:p.Gln259Pro
ENST00000346342.7:c.776A>C	ENSP00000329546.3:p.Gln259Pro
ENST00000375581.3:c.842A>C	ENSP00000364731.3:p.Gln281Pro
ENST00000541084.5:c.590A>C	ENSP00000442051.2:p.Gln197Pro
NM_000131.4:c.842A>C , LRG_554t1:c.842A>C	NP_000122.1:p.Gln281Pro
NM_001267554.1:c.590A>C	NP_001254483.1:p.Gln197Pro
NM_019616.3:c.776A>C , LRG_554t2:c.776A>C	NP_062562.1:p.Gln259Pro
NR_051961.1:n.863A>C
XM_006719963.2:c.635A>C	XP_006720026.1:p.Gln212Pro
XM_011537474.1:c.884A>C	XP_011535776.1:p.Gln295Pro
XM_011537475.1:c.698A>C	XP_011535777.1:p.Gln233Pro
XM_011537476.1:c.536A>C	XP_011535778.1:p.Gln179Pro
XM_011537477.1:c.845A>C	XP_011535779.1:p.Gln282Pro
XM_006719963.3:c.680A>C	XP_006720026.2:p.Gln227Pro
XM_011537474.2:c.929A>C	XP_011535776.2:p.Gln310Pro
XM_011537475.2:c.743A>C	XP_011535777.2:p.Gln248Pro
XM_011537476.2:c.536A>C	XP_011535778.1:p.Gln179Pro
NM_019616.4:c.776A>C MANE Select	NP_062562.1:p.Gln259Pro
NR_051961.2:n.860A>C
NM_001267554.2:c.590A>C	NP_001254483.1:p.Gln197Pro