Canonical Allele Identifier: CA388786813

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773147C>G (hg19) ; chr13:g.113118833C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118833C>G , CM000675.2:g.113118833C>G	GRCh38
NC_000013.10:g.113773147C>G , CM000675.1:g.113773147C>G	GRCh37
NC_000013.9:g.112821148C>G	NCBI36
NG_009258.1:g.1035C>G , LRG_548:g.1035C>G
NG_009262.1:g.18043C>G , LRG_554:g.18043C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1160C>G MANE Select	ENSP00000329546.4:p.Ala387Gly
ENST00000346342.7:c.1160C>G	ENSP00000329546.3:p.Ala387Gly
ENST00000375581.3:c.1226C>G	ENSP00000364731.3:p.Ala409Gly
ENST00000541084.5:c.974C>G	ENSP00000442051.2:p.Ala325Gly
NM_000131.4:c.1226C>G , LRG_554t1:c.1226C>G	NP_000122.1:p.Ala409Gly
NM_001267554.1:c.974C>G	NP_001254483.1:p.Ala325Gly
NM_019616.3:c.1160C>G , LRG_554t2:c.1160C>G	NP_062562.1:p.Ala387Gly
NR_051961.1:n.1247C>G
XM_006719963.2:c.1019C>G	XP_006720026.1:p.Ala340Gly
XM_011537474.1:c.1268C>G	XP_011535776.1:p.Ala423Gly
XM_011537475.1:c.1082C>G	XP_011535777.1:p.Ala361Gly
XM_011537476.1:c.920C>G	XP_011535778.1:p.Ala307Gly
XM_011537477.1:c.1229C>G	XP_011535779.1:p.Ala410Gly
XM_006719963.3:c.1064C>G	XP_006720026.2:p.Ala355Gly
XM_011537474.2:c.1313C>G	XP_011535776.2:p.Ala438Gly
XM_011537475.2:c.1127C>G	XP_011535777.2:p.Ala376Gly
XM_011537476.2:c.920C>G	XP_011535778.1:p.Ala307Gly
NM_019616.4:c.1160C>G MANE Select	NP_062562.1:p.Ala387Gly
NR_051961.2:n.1244C>G
NM_001267554.2:c.974C>G	NP_001254483.1:p.Ala325Gly