Canonical Allele Identifier: CA388786289

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772994T>G (hg19) ; chr13:g.113118680T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118680T>G , CM000675.2:g.113118680T>G	GRCh38
NC_000013.10:g.113772994T>G , CM000675.1:g.113772994T>G	GRCh37
NC_000013.9:g.112820995T>G	NCBI36
NG_009258.1:g.882T>G , LRG_548:g.882T>G
NG_009262.1:g.17890T>G , LRG_554:g.17890T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1007T>G MANE Select	ENSP00000329546.4:p.Met336Arg
ENST00000346342.7:c.1007T>G	ENSP00000329546.3:p.Met336Arg
ENST00000375581.3:c.1073T>G	ENSP00000364731.3:p.Met358Arg
ENST00000541084.5:c.821T>G	ENSP00000442051.2:p.Met274Arg
NM_000131.4:c.1073T>G , LRG_554t1:c.1073T>G	NP_000122.1:p.Met358Arg
NM_001267554.1:c.821T>G	NP_001254483.1:p.Met274Arg
NM_019616.3:c.1007T>G , LRG_554t2:c.1007T>G	NP_062562.1:p.Met336Arg
NR_051961.1:n.1094T>G
XM_006719963.2:c.866T>G	XP_006720026.1:p.Met289Arg
XM_011537474.1:c.1115T>G	XP_011535776.1:p.Met372Arg
XM_011537475.1:c.929T>G	XP_011535777.1:p.Met310Arg
XM_011537476.1:c.767T>G	XP_011535778.1:p.Met256Arg
XM_011537477.1:c.1076T>G	XP_011535779.1:p.Met359Arg
XM_006719963.3:c.911T>G	XP_006720026.2:p.Met304Arg
XM_011537474.2:c.1160T>G	XP_011535776.2:p.Met387Arg
XM_011537475.2:c.974T>G	XP_011535777.2:p.Met325Arg
XM_011537476.2:c.767T>G	XP_011535778.1:p.Met256Arg
NM_019616.4:c.1007T>G MANE Select	NP_062562.1:p.Met336Arg
NR_051961.2:n.1091T>G
NM_001267554.2:c.821T>G	NP_001254483.1:p.Met274Arg