Canonical Allele Identifier: CA388786805

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773146G>T (hg19) ; chr13:g.113118832G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118832G>T , CM000675.2:g.113118832G>T	GRCh38
NC_000013.10:g.113773146G>T , CM000675.1:g.113773146G>T	GRCh37
NC_000013.9:g.112821147G>T	NCBI36
NG_009258.1:g.1034G>T , LRG_548:g.1034G>T
NG_009262.1:g.18042G>T , LRG_554:g.18042G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1159G>T MANE Select	ENSP00000329546.4:p.Ala387Ser
ENST00000346342.7:c.1159G>T	ENSP00000329546.3:p.Ala387Ser
ENST00000375581.3:c.1225G>T	ENSP00000364731.3:p.Ala409Ser
ENST00000541084.5:c.973G>T	ENSP00000442051.2:p.Ala325Ser
NM_000131.4:c.1225G>T , LRG_554t1:c.1225G>T	NP_000122.1:p.Ala409Ser
NM_001267554.1:c.973G>T	NP_001254483.1:p.Ala325Ser
NM_019616.3:c.1159G>T , LRG_554t2:c.1159G>T	NP_062562.1:p.Ala387Ser
NR_051961.1:n.1246G>T
XM_006719963.2:c.1018G>T	XP_006720026.1:p.Ala340Ser
XM_011537474.1:c.1267G>T	XP_011535776.1:p.Ala423Ser
XM_011537475.1:c.1081G>T	XP_011535777.1:p.Ala361Ser
XM_011537476.1:c.919G>T	XP_011535778.1:p.Ala307Ser
XM_011537477.1:c.1228G>T	XP_011535779.1:p.Ala410Ser
XM_006719963.3:c.1063G>T	XP_006720026.2:p.Ala355Ser
XM_011537474.2:c.1312G>T	XP_011535776.2:p.Ala438Ser
XM_011537475.2:c.1126G>T	XP_011535777.2:p.Ala376Ser
XM_011537476.2:c.919G>T	XP_011535778.1:p.Ala307Ser
NM_019616.4:c.1159G>T MANE Select	NP_062562.1:p.Ala387Ser
NR_051961.2:n.1243G>T
NM_001267554.2:c.973G>T	NP_001254483.1:p.Ala325Ser