Canonical Allele Identifier: CA388786820

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773149A>T (hg19) ; chr13:g.113118835A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118835A>T , CM000675.2:g.113118835A>T	GRCh38
NC_000013.10:g.113773149A>T , CM000675.1:g.113773149A>T	GRCh37
NC_000013.9:g.112821150A>T	NCBI36
NG_009258.1:g.1037A>T , LRG_548:g.1037A>T
NG_009262.1:g.18045A>T , LRG_554:g.18045A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1162A>T MANE Select	ENSP00000329546.4:p.Thr388Ser
ENST00000346342.7:c.1162A>T	ENSP00000329546.3:p.Thr388Ser
ENST00000375581.3:c.1228A>T	ENSP00000364731.3:p.Thr410Ser
ENST00000541084.5:c.976A>T	ENSP00000442051.2:p.Thr326Ser
NM_000131.4:c.1228A>T , LRG_554t1:c.1228A>T	NP_000122.1:p.Thr410Ser
NM_001267554.1:c.976A>T	NP_001254483.1:p.Thr326Ser
NM_019616.3:c.1162A>T , LRG_554t2:c.1162A>T	NP_062562.1:p.Thr388Ser
NR_051961.1:n.1249A>T
XM_006719963.2:c.1021A>T	XP_006720026.1:p.Thr341Ser
XM_011537474.1:c.1270A>T	XP_011535776.1:p.Thr424Ser
XM_011537475.1:c.1084A>T	XP_011535777.1:p.Thr362Ser
XM_011537476.1:c.922A>T	XP_011535778.1:p.Thr308Ser
XM_011537477.1:c.1231A>T	XP_011535779.1:p.Thr411Ser
XM_006719963.3:c.1066A>T	XP_006720026.2:p.Thr356Ser
XM_011537474.2:c.1315A>T	XP_011535776.2:p.Thr439Ser
XM_011537475.2:c.1129A>T	XP_011535777.2:p.Thr377Ser
XM_011537476.2:c.922A>T	XP_011535778.1:p.Thr308Ser
NM_019616.4:c.1162A>T MANE Select	NP_062562.1:p.Thr388Ser
NR_051961.2:n.1246A>T
NM_001267554.2:c.976A>T	NP_001254483.1:p.Thr326Ser