Canonical Allele Identifier: CA485021833

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773322G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119008G>A , CM000675.2:g.113119008G>A	GRCh38
NC_000013.10:g.113773322G>A , CM000675.1:g.113773322G>A	GRCh37
NC_000013.9:g.112821323G>A	NCBI36
NG_009258.1:g.1210G>A , LRG_548:g.1210G>A
NG_009262.1:g.18218G>A , LRG_554:g.18218G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1335G>A MANE Select	ENSP00000329546.4:p.Ter445=
ENST00000346342.7:c.1335G>A	ENSP00000329546.3:p.Ter445=
ENST00000375581.3:c.1401G>A	ENSP00000364731.3:p.Ter467=
ENST00000541084.5:c.1149G>A	ENSP00000442051.2:p.Ter383=
NM_000131.4:c.1401G>A , LRG_554t1:c.1401G>A	NP_000122.1:p.Ter467=
NM_001267554.1:c.1149G>A	NP_001254483.1:p.Ter383=
NM_019616.3:c.1335G>A , LRG_554t2:c.1335G>A	NP_062562.1:p.Ter445=
NR_051961.1:n.1422G>A
XM_006719963.2:c.1194G>A	XP_006720026.1:p.Ter398=
XM_011537474.1:c.1443G>A	XP_011535776.1:p.Ter481=
XM_011537475.1:c.1257G>A	XP_011535777.1:p.Ter419=
XM_011537476.1:c.1095G>A	XP_011535778.1:p.Ter365=
XM_011537477.1:c.1404G>A	XP_011535779.1:p.Ter468=
XM_006719963.3:c.1239G>A	XP_006720026.2:p.Ter413=
XM_011537474.2:c.1488G>A	XP_011535776.2:p.Ter496=
XM_011537475.2:c.1302G>A	XP_011535777.2:p.Ter434=
XM_011537476.2:c.1095G>A	XP_011535778.1:p.Ter365=
NM_019616.4:c.1335G>A MANE Select	NP_062562.1:p.Ter445=
NR_051961.2:n.1419G>A
NM_001267554.2:c.1149G>A	NP_001254483.1:p.Ter383=