Canonical Allele Identifier: CA388786620

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773105G>T (hg19) ; chr13:g.113118791G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118791G>T , CM000675.2:g.113118791G>T	GRCh38
NC_000013.10:g.113773105G>T , CM000675.1:g.113773105G>T	GRCh37
NC_000013.9:g.112821106G>T	NCBI36
NG_009258.1:g.993G>T , LRG_548:g.993G>T
NG_009262.1:g.18001G>T , LRG_554:g.18001G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1118G>T MANE Select	ENSP00000329546.4:p.Gly373Val
ENST00000346342.7:c.1118G>T	ENSP00000329546.3:p.Gly373Val
ENST00000375581.3:c.1184G>T	ENSP00000364731.3:p.Gly395Val
ENST00000541084.5:c.932G>T	ENSP00000442051.2:p.Gly311Val
NM_000131.4:c.1184G>T , LRG_554t1:c.1184G>T	NP_000122.1:p.Gly395Val
NM_001267554.1:c.932G>T	NP_001254483.1:p.Gly311Val
NM_019616.3:c.1118G>T , LRG_554t2:c.1118G>T	NP_062562.1:p.Gly373Val
NR_051961.1:n.1205G>T
XM_006719963.2:c.977G>T	XP_006720026.1:p.Gly326Val
XM_011537474.1:c.1226G>T	XP_011535776.1:p.Gly409Val
XM_011537475.1:c.1040G>T	XP_011535777.1:p.Gly347Val
XM_011537476.1:c.878G>T	XP_011535778.1:p.Gly293Val
XM_011537477.1:c.1187G>T	XP_011535779.1:p.Gly396Val
XM_006719963.3:c.1022G>T	XP_006720026.2:p.Gly341Val
XM_011537474.2:c.1271G>T	XP_011535776.2:p.Gly424Val
XM_011537475.2:c.1085G>T	XP_011535777.2:p.Gly362Val
XM_011537476.2:c.878G>T	XP_011535778.1:p.Gly293Val
NM_019616.4:c.1118G>T MANE Select	NP_062562.1:p.Gly373Val
NR_051961.2:n.1202G>T
NM_001267554.2:c.932G>T	NP_001254483.1:p.Gly311Val