Canonical Allele Identifier: CA388787166

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773278T>A (hg19) ; chr13:g.113118964T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118964T>A , CM000675.2:g.113118964T>A	GRCh38
NC_000013.10:g.113773278T>A , CM000675.1:g.113773278T>A	GRCh37
NC_000013.9:g.112821279T>A	NCBI36
NG_009258.1:g.1166T>A , LRG_548:g.1166T>A
NG_009262.1:g.18174T>A , LRG_554:g.18174T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1291T>A MANE Select	ENSP00000329546.4:p.Ser431Thr
ENST00000346342.7:c.1291T>A	ENSP00000329546.3:p.Ser431Thr
ENST00000375581.3:c.1357T>A	ENSP00000364731.3:p.Ser453Thr
ENST00000541084.5:c.1105T>A	ENSP00000442051.2:p.Ser369Thr
NM_000131.4:c.1357T>A , LRG_554t1:c.1357T>A	NP_000122.1:p.Ser453Thr
NM_001267554.1:c.1105T>A	NP_001254483.1:p.Ser369Thr
NM_019616.3:c.1291T>A , LRG_554t2:c.1291T>A	NP_062562.1:p.Ser431Thr
NR_051961.1:n.1378T>A
XM_006719963.2:c.1150T>A	XP_006720026.1:p.Ser384Thr
XM_011537474.1:c.1399T>A	XP_011535776.1:p.Ser467Thr
XM_011537475.1:c.1213T>A	XP_011535777.1:p.Ser405Thr
XM_011537476.1:c.1051T>A	XP_011535778.1:p.Ser351Thr
XM_011537477.1:c.1360T>A	XP_011535779.1:p.Ser454Thr
XM_006719963.3:c.1195T>A	XP_006720026.2:p.Ser399Thr
XM_011537474.2:c.1444T>A	XP_011535776.2:p.Ser482Thr
XM_011537475.2:c.1258T>A	XP_011535777.2:p.Ser420Thr
XM_011537476.2:c.1051T>A	XP_011535778.1:p.Ser351Thr
NM_019616.4:c.1291T>A MANE Select	NP_062562.1:p.Ser431Thr
NR_051961.2:n.1375T>A
NM_001267554.2:c.1105T>A	NP_001254483.1:p.Ser369Thr