Canonical Allele Identifier: CA485423941

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772929G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118615G>T , CM000675.2:g.113118615G>T	GRCh38
NC_000013.10:g.113772929G>T , CM000675.1:g.113772929G>T	GRCh37
NC_000013.9:g.112820930G>T	NCBI36
NG_009258.1:g.817G>T , LRG_548:g.817G>T
NG_009262.1:g.17825G>T , LRG_554:g.17825G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.942G>T MANE Select	ENSP00000329546.4:p.Val314=
ENST00000346342.7:c.942G>T	ENSP00000329546.3:p.Val314=
ENST00000375581.3:c.1008G>T	ENSP00000364731.3:p.Val336=
ENST00000541084.5:c.756G>T	ENSP00000442051.2:p.Val252=
NM_000131.4:c.1008G>T , LRG_554t1:c.1008G>T	NP_000122.1:p.Val336=
NM_001267554.1:c.756G>T	NP_001254483.1:p.Val252=
NM_019616.3:c.942G>T , LRG_554t2:c.942G>T	NP_062562.1:p.Val314=
NR_051961.1:n.1029G>T
XM_006719963.2:c.801G>T	XP_006720026.1:p.Val267=
XM_011537474.1:c.1050G>T	XP_011535776.1:p.Val350=
XM_011537475.1:c.864G>T	XP_011535777.1:p.Val288=
XM_011537476.1:c.702G>T	XP_011535778.1:p.Val234=
XM_011537477.1:c.1011G>T	XP_011535779.1:p.Val337=
XM_006719963.3:c.846G>T	XP_006720026.2:p.Val282=
XM_011537474.2:c.1095G>T	XP_011535776.2:p.Val365=
XM_011537475.2:c.909G>T	XP_011535777.2:p.Val303=
XM_011537476.2:c.702G>T	XP_011535778.1:p.Val234=
NM_019616.4:c.942G>T MANE Select	NP_062562.1:p.Val314=
NR_051961.2:n.1026G>T
NM_001267554.2:c.756G>T	NP_001254483.1:p.Val252=