Canonical Allele Identifier: CA388786337

Gene: F7

Linked Data

• dbSNP Id: rs747673406
• MyVariant Identifiers: chr13:g.113773020A>C (hg19) ; chr13:g.113118706A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118706A>C , CM000675.2:g.113118706A>C	GRCh38
NC_000013.10:g.113773020A>C , CM000675.1:g.113773020A>C	GRCh37
NC_000013.9:g.112821021A>C	NCBI36
NG_009258.1:g.908A>C , LRG_548:g.908A>C
NG_009262.1:g.17916A>C , LRG_554:g.17916A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1033A>C MANE Select	ENSP00000329546.4:p.Thr345Pro
ENST00000346342.7:c.1033A>C	ENSP00000329546.3:p.Thr345Pro
ENST00000375581.3:c.1099A>C	ENSP00000364731.3:p.Thr367Pro
ENST00000541084.5:c.847A>C	ENSP00000442051.2:p.Thr283Pro
NM_000131.4:c.1099A>C , LRG_554t1:c.1099A>C	NP_000122.1:p.Thr367Pro
NM_001267554.1:c.847A>C	NP_001254483.1:p.Thr283Pro
NM_019616.3:c.1033A>C , LRG_554t2:c.1033A>C	NP_062562.1:p.Thr345Pro
NR_051961.1:n.1120A>C
XM_006719963.2:c.892A>C	XP_006720026.1:p.Thr298Pro
XM_011537474.1:c.1141A>C	XP_011535776.1:p.Thr381Pro
XM_011537475.1:c.955A>C	XP_011535777.1:p.Thr319Pro
XM_011537476.1:c.793A>C	XP_011535778.1:p.Thr265Pro
XM_011537477.1:c.1102A>C	XP_011535779.1:p.Thr368Pro
XM_006719963.3:c.937A>C	XP_006720026.2:p.Thr313Pro
XM_011537474.2:c.1186A>C	XP_011535776.2:p.Thr396Pro
XM_011537475.2:c.1000A>C	XP_011535777.2:p.Thr334Pro
XM_011537476.2:c.793A>C	XP_011535778.1:p.Thr265Pro
NM_019616.4:c.1033A>C MANE Select	NP_062562.1:p.Thr345Pro
NR_051961.2:n.1117A>C
NM_001267554.2:c.847A>C	NP_001254483.1:p.Thr283Pro