Canonical Allele Identifier: CA2120142716

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118810G= , CM000675.2:g.113118810G=	GRCh38
NC_000013.10:g.113773124G= , CM000675.1:g.113773124G=	GRCh37
NC_000013.9:g.112821125G=	NCBI36
NG_009258.1:g.1012G= , LRG_548:g.1012G=
NG_009262.1:g.18020G= , LRG_554:g.18020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1137G= MANE Select	ENSP00000329546.4:p.Lys379=
ENST00000346342.7:c.1137G=	ENSP00000329546.3:p.Lys379=
ENST00000375581.3:c.1203G=	ENSP00000364731.3:p.Lys401=
ENST00000541084.5:c.951G=	ENSP00000442051.2:p.Lys317=
NM_000131.4:c.1203G= , LRG_554t1:c.1203G=	NP_000122.1:p.Lys401=
NM_001267554.1:c.951G=	NP_001254483.1:p.Lys317=
NM_019616.3:c.1137G= , LRG_554t2:c.1137G=	NP_062562.1:p.Lys379=
NR_051961.1:n.1224G=
XM_006719963.2:c.996G=	XP_006720026.1:p.Lys332=
XM_011537474.1:c.1245G=	XP_011535776.1:p.Lys415=
XM_011537475.1:c.1059G=	XP_011535777.1:p.Lys353=
XM_011537476.1:c.897G=	XP_011535778.1:p.Lys299=
XM_011537477.1:c.1206G=	XP_011535779.1:p.Lys402=
XM_006719963.3:c.1041G=	XP_006720026.2:p.Lys347=
XM_011537474.2:c.1290G=	XP_011535776.2:p.Lys430=
XM_011537475.2:c.1104G=	XP_011535777.2:p.Lys368=
XM_011537476.2:c.897G=	XP_011535778.1:p.Lys299=
NM_019616.4:c.1137G= MANE Select	NP_062562.1:p.Lys379=
NR_051961.2:n.1221G=
NM_001267554.2:c.951G=	NP_001254483.1:p.Lys317=