Canonical Allele Identifier: CA2120142757

Gene: F7

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1162A= MANE Select	ENSP00000329546.4:p.Thr388=
ENST00000346342.7:c.1162A=	ENSP00000329546.3:p.Thr388=
ENST00000375581.3:c.1228A=	ENSP00000364731.3:p.Thr410=
ENST00000541084.5:c.976A=	ENSP00000442051.2:p.Thr326=
NM_000131.4:c.1228A= , LRG_554t1:c.1228A=	NP_000122.1:p.Thr410=
NM_001267554.1:c.976A=	NP_001254483.1:p.Thr326=
NM_019616.3:c.1162A= , LRG_554t2:c.1162A=	NP_062562.1:p.Thr388=
NR_051961.1:n.1249A=
XM_006719963.2:c.1021A=	XP_006720026.1:p.Thr341=
XM_011537474.1:c.1270A=	XP_011535776.1:p.Thr424=
XM_011537475.1:c.1084A=	XP_011535777.1:p.Thr362=
XM_011537476.1:c.922A=	XP_011535778.1:p.Thr308=
XM_011537477.1:c.1231A=	XP_011535779.1:p.Thr411=
XM_006719963.3:c.1066A=	XP_006720026.2:p.Thr356=
XM_011537474.2:c.1315A=	XP_011535776.2:p.Thr439=
XM_011537475.2:c.1129A=	XP_011535777.2:p.Thr377=
XM_011537476.2:c.922A=	XP_011535778.1:p.Thr308=
NM_019616.4:c.1162A= MANE Select	NP_062562.1:p.Thr388=
NR_051961.2:n.1246A=
NM_001267554.2:c.976A=	NP_001254483.1:p.Thr326=