Canonical Allele Identifier: CA388785949

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772820A>C (hg19) ; chr13:g.113118506A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118506A>C , CM000675.2:g.113118506A>C	GRCh38
NC_000013.10:g.113772820A>C , CM000675.1:g.113772820A>C	GRCh37
NC_000013.9:g.112820821A>C	NCBI36
NG_009258.1:g.708A>C , LRG_548:g.708A>C
NG_009262.1:g.17716A>C , LRG_554:g.17716A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.833A>C MANE Select	ENSP00000329546.4:p.Asn278Thr
ENST00000346342.7:c.833A>C	ENSP00000329546.3:p.Asn278Thr
ENST00000375581.3:c.899A>C	ENSP00000364731.3:p.Asn300Thr
ENST00000541084.5:c.647A>C	ENSP00000442051.2:p.Asn216Thr
NM_000131.4:c.899A>C , LRG_554t1:c.899A>C	NP_000122.1:p.Asn300Thr
NM_001267554.1:c.647A>C	NP_001254483.1:p.Asn216Thr
NM_019616.3:c.833A>C , LRG_554t2:c.833A>C	NP_062562.1:p.Asn278Thr
NR_051961.1:n.920A>C
XM_006719963.2:c.692A>C	XP_006720026.1:p.Asn231Thr
XM_011537474.1:c.941A>C	XP_011535776.1:p.Asn314Thr
XM_011537475.1:c.755A>C	XP_011535777.1:p.Asn252Thr
XM_011537476.1:c.593A>C	XP_011535778.1:p.Asn198Thr
XM_011537477.1:c.902A>C	XP_011535779.1:p.Asn301Thr
XM_006719963.3:c.737A>C	XP_006720026.2:p.Asn246Thr
XM_011537474.2:c.986A>C	XP_011535776.2:p.Asn329Thr
XM_011537475.2:c.800A>C	XP_011535777.2:p.Asn267Thr
XM_011537476.2:c.593A>C	XP_011535778.1:p.Asn198Thr
NM_019616.4:c.833A>C MANE Select	NP_062562.1:p.Asn278Thr
NR_051961.2:n.917A>C
NM_001267554.2:c.647A>C	NP_001254483.1:p.Asn216Thr