Canonical Allele Identifier: CA388786633

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773109C>A (hg19) ; chr13:g.113118795C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118795C>A , CM000675.2:g.113118795C>A	GRCh38
NC_000013.10:g.113773109C>A , CM000675.1:g.113773109C>A	GRCh37
NC_000013.9:g.112821110C>A	NCBI36
NG_009258.1:g.997C>A , LRG_548:g.997C>A
NG_009262.1:g.18005C>A , LRG_554:g.18005C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1122C>A MANE Select	ENSP00000329546.4:p.Ser374Arg
ENST00000346342.7:c.1122C>A	ENSP00000329546.3:p.Ser374Arg
ENST00000375581.3:c.1188C>A	ENSP00000364731.3:p.Ser396Arg
ENST00000541084.5:c.936C>A	ENSP00000442051.2:p.Ser312Arg
NM_000131.4:c.1188C>A , LRG_554t1:c.1188C>A	NP_000122.1:p.Ser396Arg
NM_001267554.1:c.936C>A	NP_001254483.1:p.Ser312Arg
NM_019616.3:c.1122C>A , LRG_554t2:c.1122C>A	NP_062562.1:p.Ser374Arg
NR_051961.1:n.1209C>A
XM_006719963.2:c.981C>A	XP_006720026.1:p.Ser327Arg
XM_011537474.1:c.1230C>A	XP_011535776.1:p.Ser410Arg
XM_011537475.1:c.1044C>A	XP_011535777.1:p.Ser348Arg
XM_011537476.1:c.882C>A	XP_011535778.1:p.Ser294Arg
XM_011537477.1:c.1191C>A	XP_011535779.1:p.Ser397Arg
XM_006719963.3:c.1026C>A	XP_006720026.2:p.Ser342Arg
XM_011537474.2:c.1275C>A	XP_011535776.2:p.Ser425Arg
XM_011537475.2:c.1089C>A	XP_011535777.2:p.Ser363Arg
XM_011537476.2:c.882C>A	XP_011535778.1:p.Ser294Arg
NM_019616.4:c.1122C>A MANE Select	NP_062562.1:p.Ser374Arg
NR_051961.2:n.1206C>A
NM_001267554.2:c.936C>A	NP_001254483.1:p.Ser312Arg