Canonical Allele Identifier: CA388787170

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773279C>G (hg19) ; chr13:g.113118965C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118965C>G , CM000675.2:g.113118965C>G	GRCh38
NC_000013.10:g.113773279C>G , CM000675.1:g.113773279C>G	GRCh37
NC_000013.9:g.112821280C>G	NCBI36
NG_009258.1:g.1167C>G , LRG_548:g.1167C>G
NG_009262.1:g.18175C>G , LRG_554:g.18175C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1292C>G MANE Select	ENSP00000329546.4:p.Ser431Ter
ENST00000346342.7:c.1292C>G	ENSP00000329546.3:p.Ser431Ter
ENST00000375581.3:c.1358C>G	ENSP00000364731.3:p.Ser453Ter
ENST00000541084.5:c.1106C>G	ENSP00000442051.2:p.Ser369Ter
NM_000131.4:c.1358C>G , LRG_554t1:c.1358C>G	NP_000122.1:p.Ser453Ter
NM_001267554.1:c.1106C>G	NP_001254483.1:p.Ser369Ter
NM_019616.3:c.1292C>G , LRG_554t2:c.1292C>G	NP_062562.1:p.Ser431Ter
NR_051961.1:n.1379C>G
XM_006719963.2:c.1151C>G	XP_006720026.1:p.Ser384Ter
XM_011537474.1:c.1400C>G	XP_011535776.1:p.Ser467Ter
XM_011537475.1:c.1214C>G	XP_011535777.1:p.Ser405Ter
XM_011537476.1:c.1052C>G	XP_011535778.1:p.Ser351Ter
XM_011537477.1:c.1361C>G	XP_011535779.1:p.Ser454Ter
XM_006719963.3:c.1196C>G	XP_006720026.2:p.Ser399Ter
XM_011537474.2:c.1445C>G	XP_011535776.2:p.Ser482Ter
XM_011537475.2:c.1259C>G	XP_011535777.2:p.Ser420Ter
XM_011537476.2:c.1052C>G	XP_011535778.1:p.Ser351Ter
NM_019616.4:c.1292C>G MANE Select	NP_062562.1:p.Ser431Ter
NR_051961.2:n.1376C>G
NM_001267554.2:c.1106C>G	NP_001254483.1:p.Ser369Ter