Canonical Allele Identifier: CA485021184

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773115C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118801C>T , CM000675.2:g.113118801C>T	GRCh38
NC_000013.10:g.113773115C>T , CM000675.1:g.113773115C>T	GRCh37
NC_000013.9:g.112821116C>T	NCBI36
NG_009258.1:g.1003C>T , LRG_548:g.1003C>T
NG_009262.1:g.18011C>T , LRG_554:g.18011C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1128C>T MANE Select	ENSP00000329546.4:p.Asp376=
ENST00000346342.7:c.1128C>T	ENSP00000329546.3:p.Asp376=
ENST00000375581.3:c.1194C>T	ENSP00000364731.3:p.Asp398=
ENST00000541084.5:c.942C>T	ENSP00000442051.2:p.Asp314=
NM_000131.4:c.1194C>T , LRG_554t1:c.1194C>T	NP_000122.1:p.Asp398=
NM_001267554.1:c.942C>T	NP_001254483.1:p.Asp314=
NM_019616.3:c.1128C>T , LRG_554t2:c.1128C>T	NP_062562.1:p.Asp376=
NR_051961.1:n.1215C>T
XM_006719963.2:c.987C>T	XP_006720026.1:p.Asp329=
XM_011537474.1:c.1236C>T	XP_011535776.1:p.Asp412=
XM_011537475.1:c.1050C>T	XP_011535777.1:p.Asp350=
XM_011537476.1:c.888C>T	XP_011535778.1:p.Asp296=
XM_011537477.1:c.1197C>T	XP_011535779.1:p.Asp399=
XM_006719963.3:c.1032C>T	XP_006720026.2:p.Asp344=
XM_011537474.2:c.1281C>T	XP_011535776.2:p.Asp427=
XM_011537475.2:c.1095C>T	XP_011535777.2:p.Asp365=
XM_011537476.2:c.888C>T	XP_011535778.1:p.Asp296=
NM_019616.4:c.1128C>T MANE Select	NP_062562.1:p.Asp376=
NR_051961.2:n.1212C>T
NM_001267554.2:c.942C>T	NP_001254483.1:p.Asp314=