Canonical Allele Identifier: CA388787231

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773315T>C (hg19) ; chr13:g.113119001T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119001T>C , CM000675.2:g.113119001T>C	GRCh38
NC_000013.10:g.113773315T>C , CM000675.1:g.113773315T>C	GRCh37
NC_000013.9:g.112821316T>C	NCBI36
NG_009258.1:g.1203T>C , LRG_548:g.1203T>C
NG_009262.1:g.18211T>C , LRG_554:g.18211T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1328T>C MANE Select	ENSP00000329546.4:p.Phe443Ser
ENST00000346342.7:c.1328T>C	ENSP00000329546.3:p.Phe443Ser
ENST00000375581.3:c.1394T>C	ENSP00000364731.3:p.Phe465Ser
ENST00000541084.5:c.1142T>C	ENSP00000442051.2:p.Phe381Ser
NM_000131.4:c.1394T>C , LRG_554t1:c.1394T>C	NP_000122.1:p.Phe465Ser
NM_001267554.1:c.1142T>C	NP_001254483.1:p.Phe381Ser
NM_019616.3:c.1328T>C , LRG_554t2:c.1328T>C	NP_062562.1:p.Phe443Ser
NR_051961.1:n.1415T>C
XM_006719963.2:c.1187T>C	XP_006720026.1:p.Phe396Ser
XM_011537474.1:c.1436T>C	XP_011535776.1:p.Phe479Ser
XM_011537475.1:c.1250T>C	XP_011535777.1:p.Phe417Ser
XM_011537476.1:c.1088T>C	XP_011535778.1:p.Phe363Ser
XM_011537477.1:c.1397T>C	XP_011535779.1:p.Phe466Ser
XM_006719963.3:c.1232T>C	XP_006720026.2:p.Phe411Ser
XM_011537474.2:c.1481T>C	XP_011535776.2:p.Phe494Ser
XM_011537475.2:c.1295T>C	XP_011535777.2:p.Phe432Ser
XM_011537476.2:c.1088T>C	XP_011535778.1:p.Phe363Ser
NM_019616.4:c.1328T>C MANE Select	NP_062562.1:p.Phe443Ser
NR_051961.2:n.1412T>C
NM_001267554.2:c.1142T>C	NP_001254483.1:p.Phe381Ser