Canonical Allele Identifier: CA388786194

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772946G>T (hg19) ; chr13:g.113118632G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118632G>T , CM000675.2:g.113118632G>T	GRCh38
NC_000013.10:g.113772946G>T , CM000675.1:g.113772946G>T	GRCh37
NC_000013.9:g.112820947G>T	NCBI36
NG_009258.1:g.834G>T , LRG_548:g.834G>T
NG_009262.1:g.17842G>T , LRG_554:g.17842G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.959G>T MANE Select	ENSP00000329546.4:p.Ser320Ile
ENST00000346342.7:c.959G>T	ENSP00000329546.3:p.Ser320Ile
ENST00000375581.3:c.1025G>T	ENSP00000364731.3:p.Ser342Ile
ENST00000541084.5:c.773G>T	ENSP00000442051.2:p.Ser258Ile
NM_000131.4:c.1025G>T , LRG_554t1:c.1025G>T	NP_000122.1:p.Ser342Ile
NM_001267554.1:c.773G>T	NP_001254483.1:p.Ser258Ile
NM_019616.3:c.959G>T , LRG_554t2:c.959G>T	NP_062562.1:p.Ser320Ile
NR_051961.1:n.1046G>T
XM_006719963.2:c.818G>T	XP_006720026.1:p.Ser273Ile
XM_011537474.1:c.1067G>T	XP_011535776.1:p.Ser356Ile
XM_011537475.1:c.881G>T	XP_011535777.1:p.Ser294Ile
XM_011537476.1:c.719G>T	XP_011535778.1:p.Ser240Ile
XM_011537477.1:c.1028G>T	XP_011535779.1:p.Ser343Ile
XM_006719963.3:c.863G>T	XP_006720026.2:p.Ser288Ile
XM_011537474.2:c.1112G>T	XP_011535776.2:p.Ser371Ile
XM_011537475.2:c.926G>T	XP_011535777.2:p.Ser309Ile
XM_011537476.2:c.719G>T	XP_011535778.1:p.Ser240Ile
NM_019616.4:c.959G>T MANE Select	NP_062562.1:p.Ser320Ile
NR_051961.2:n.1043G>T
NM_001267554.2:c.773G>T	NP_001254483.1:p.Ser258Ile