Canonical Allele Identifier: CA2120143075

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118976C= , CM000675.2:g.113118976C=	GRCh38
NC_000013.10:g.113773290C= , CM000675.1:g.113773290C=	GRCh37
NC_000013.9:g.112821291C=	NCBI36
NG_009258.1:g.1178C= , LRG_548:g.1178C=
NG_009262.1:g.18186C= , LRG_554:g.18186C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1303C= MANE Select	ENSP00000329546.4:p.Pro435=
ENST00000346342.7:c.1303C=	ENSP00000329546.3:p.Pro435=
ENST00000375581.3:c.1369C=	ENSP00000364731.3:p.Pro457=
ENST00000541084.5:c.1117C=	ENSP00000442051.2:p.Pro373=
NM_000131.4:c.1369C= , LRG_554t1:c.1369C=	NP_000122.1:p.Pro457=
NM_001267554.1:c.1117C=	NP_001254483.1:p.Pro373=
NM_019616.3:c.1303C= , LRG_554t2:c.1303C=	NP_062562.1:p.Pro435=
NR_051961.1:n.1390C=
XM_006719963.2:c.1162C=	XP_006720026.1:p.Pro388=
XM_011537474.1:c.1411C=	XP_011535776.1:p.Pro471=
XM_011537475.1:c.1225C=	XP_011535777.1:p.Pro409=
XM_011537476.1:c.1063C=	XP_011535778.1:p.Pro355=
XM_011537477.1:c.1372C=	XP_011535779.1:p.Pro458=
XM_006719963.3:c.1207C=	XP_006720026.2:p.Pro403=
XM_011537474.2:c.1456C=	XP_011535776.2:p.Pro486=
XM_011537475.2:c.1270C=	XP_011535777.2:p.Pro424=
XM_011537476.2:c.1063C=	XP_011535778.1:p.Pro355=
NM_019616.4:c.1303C= MANE Select	NP_062562.1:p.Pro435=
NR_051961.2:n.1387C=
NM_001267554.2:c.1117C=	NP_001254483.1:p.Pro373=