Canonical Allele Identifier: CA485423866

Gene: F7

Linked Data

• gnomAD v4: 13-113118504-C-G
• MyVariant Identifiers: chr13:g.113772818C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118504C>G , CM000675.2:g.113118504C>G	GRCh38
NC_000013.10:g.113772818C>G , CM000675.1:g.113772818C>G	GRCh37
NC_000013.9:g.112820819C>G	NCBI36
NG_009258.1:g.706C>G , LRG_548:g.706C>G
NG_009262.1:g.17714C>G , LRG_554:g.17714C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.831C>G MANE Select	ENSP00000329546.4:p.Thr277=
ENST00000346342.7:c.831C>G	ENSP00000329546.3:p.Thr277=
ENST00000375581.3:c.897C>G	ENSP00000364731.3:p.Thr299=
ENST00000541084.5:c.645C>G	ENSP00000442051.2:p.Thr215=
NM_000131.4:c.897C>G , LRG_554t1:c.897C>G	NP_000122.1:p.Thr299=
NM_001267554.1:c.645C>G	NP_001254483.1:p.Thr215=
NM_019616.3:c.831C>G , LRG_554t2:c.831C>G	NP_062562.1:p.Thr277=
NR_051961.1:n.918C>G
XM_006719963.2:c.690C>G	XP_006720026.1:p.Thr230=
XM_011537474.1:c.939C>G	XP_011535776.1:p.Thr313=
XM_011537475.1:c.753C>G	XP_011535777.1:p.Thr251=
XM_011537476.1:c.591C>G	XP_011535778.1:p.Thr197=
XM_011537477.1:c.900C>G	XP_011535779.1:p.Thr300=
XM_006719963.3:c.735C>G	XP_006720026.2:p.Thr245=
XM_011537474.2:c.984C>G	XP_011535776.2:p.Thr328=
XM_011537475.2:c.798C>G	XP_011535777.2:p.Thr266=
XM_011537476.2:c.591C>G	XP_011535778.1:p.Thr197=
NM_019616.4:c.831C>G MANE Select	NP_062562.1:p.Thr277=
NR_051961.2:n.915C>G
NM_001267554.2:c.645C>G	NP_001254483.1:p.Thr215=