Canonical Allele Identifier: CA485423986

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772998C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118684C>T , CM000675.2:g.113118684C>T	GRCh38
NC_000013.10:g.113772998C>T , CM000675.1:g.113772998C>T	GRCh37
NC_000013.9:g.112820999C>T	NCBI36
NG_009258.1:g.886C>T , LRG_548:g.886C>T
NG_009262.1:g.17894C>T , LRG_554:g.17894C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1011C>T MANE Select	ENSP00000329546.4:p.Val337=
ENST00000346342.7:c.1011C>T	ENSP00000329546.3:p.Val337=
ENST00000375581.3:c.1077C>T	ENSP00000364731.3:p.Val359=
ENST00000541084.5:c.825C>T	ENSP00000442051.2:p.Val275=
NM_000131.4:c.1077C>T , LRG_554t1:c.1077C>T	NP_000122.1:p.Val359=
NM_001267554.1:c.825C>T	NP_001254483.1:p.Val275=
NM_019616.3:c.1011C>T , LRG_554t2:c.1011C>T	NP_062562.1:p.Val337=
NR_051961.1:n.1098C>T
XM_006719963.2:c.870C>T	XP_006720026.1:p.Val290=
XM_011537474.1:c.1119C>T	XP_011535776.1:p.Val373=
XM_011537475.1:c.933C>T	XP_011535777.1:p.Val311=
XM_011537476.1:c.771C>T	XP_011535778.1:p.Val257=
XM_011537477.1:c.1080C>T	XP_011535779.1:p.Val360=
XM_006719963.3:c.915C>T	XP_006720026.2:p.Val305=
XM_011537474.2:c.1164C>T	XP_011535776.2:p.Val388=
XM_011537475.2:c.978C>T	XP_011535777.2:p.Val326=
XM_011537476.2:c.771C>T	XP_011535778.1:p.Val257=
NM_019616.4:c.1011C>T MANE Select	NP_062562.1:p.Val337=
NR_051961.2:n.1095C>T
NM_001267554.2:c.825C>T	NP_001254483.1:p.Val275=