Canonical Allele Identifier: CA388786161

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772930C>A (hg19) ; chr13:g.113118616C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118616C>A , CM000675.2:g.113118616C>A	GRCh38
NC_000013.10:g.113772930C>A , CM000675.1:g.113772930C>A	GRCh37
NC_000013.9:g.112820931C>A	NCBI36
NG_009258.1:g.818C>A , LRG_548:g.818C>A
NG_009262.1:g.17826C>A , LRG_554:g.17826C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.943C>A MANE Select	ENSP00000329546.4:p.Arg315Ser
ENST00000346342.7:c.943C>A	ENSP00000329546.3:p.Arg315Ser
ENST00000375581.3:c.1009C>A	ENSP00000364731.3:p.Arg337Ser
ENST00000541084.5:c.757C>A	ENSP00000442051.2:p.Arg253Ser
NM_000131.4:c.1009C>A , LRG_554t1:c.1009C>A	NP_000122.1:p.Arg337Ser
NM_001267554.1:c.757C>A	NP_001254483.1:p.Arg253Ser
NM_019616.3:c.943C>A , LRG_554t2:c.943C>A	NP_062562.1:p.Arg315Ser
NR_051961.1:n.1030C>A
XM_006719963.2:c.802C>A	XP_006720026.1:p.Arg268Ser
XM_011537474.1:c.1051C>A	XP_011535776.1:p.Arg351Ser
XM_011537475.1:c.865C>A	XP_011535777.1:p.Arg289Ser
XM_011537476.1:c.703C>A	XP_011535778.1:p.Arg235Ser
XM_011537477.1:c.1012C>A	XP_011535779.1:p.Arg338Ser
XM_006719963.3:c.847C>A	XP_006720026.2:p.Arg283Ser
XM_011537474.2:c.1096C>A	XP_011535776.2:p.Arg366Ser
XM_011537475.2:c.910C>A	XP_011535777.2:p.Arg304Ser
XM_011537476.2:c.703C>A	XP_011535778.1:p.Arg235Ser
NM_019616.4:c.943C>A MANE Select	NP_062562.1:p.Arg315Ser
NR_051961.2:n.1027C>A
NM_001267554.2:c.757C>A	NP_001254483.1:p.Arg253Ser