Canonical Allele Identifier: CA485021208

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773151C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118837C>T , CM000675.2:g.113118837C>T	GRCh38
NC_000013.10:g.113773151C>T , CM000675.1:g.113773151C>T	GRCh37
NC_000013.9:g.112821152C>T	NCBI36
NG_009258.1:g.1039C>T , LRG_548:g.1039C>T
NG_009262.1:g.18047C>T , LRG_554:g.18047C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1164C>T MANE Select	ENSP00000329546.4:p.Thr388=
ENST00000346342.7:c.1164C>T	ENSP00000329546.3:p.Thr388=
ENST00000375581.3:c.1230C>T	ENSP00000364731.3:p.Thr410=
ENST00000541084.5:c.978C>T	ENSP00000442051.2:p.Thr326=
NM_000131.4:c.1230C>T , LRG_554t1:c.1230C>T	NP_000122.1:p.Thr410=
NM_001267554.1:c.978C>T	NP_001254483.1:p.Thr326=
NM_019616.3:c.1164C>T , LRG_554t2:c.1164C>T	NP_062562.1:p.Thr388=
NR_051961.1:n.1251C>T
XM_006719963.2:c.1023C>T	XP_006720026.1:p.Thr341=
XM_011537474.1:c.1272C>T	XP_011535776.1:p.Thr424=
XM_011537475.1:c.1086C>T	XP_011535777.1:p.Thr362=
XM_011537476.1:c.924C>T	XP_011535778.1:p.Thr308=
XM_011537477.1:c.1233C>T	XP_011535779.1:p.Thr411=
XM_006719963.3:c.1068C>T	XP_006720026.2:p.Thr356=
XM_011537474.2:c.1317C>T	XP_011535776.2:p.Thr439=
XM_011537475.2:c.1131C>T	XP_011535777.2:p.Thr377=
XM_011537476.2:c.924C>T	XP_011535778.1:p.Thr308=
NM_019616.4:c.1164C>T MANE Select	NP_062562.1:p.Thr388=
NR_051961.2:n.1248C>T
NM_001267554.2:c.978C>T	NP_001254483.1:p.Thr326=