Canonical Allele Identifier: CA2120135446

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113795C= , CM000675.2:g.113113795C=	GRCh38
NC_000013.10:g.113768109C= , CM000675.1:g.113768109C=	GRCh37
NC_000013.9:g.112816110C=	NCBI36
NG_009262.1:g.13005C= , LRG_554:g.13005C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.250+19C= MANE Select	ENSP00000329546.4:n.250+19C=
ENST00000346342.7:c.250+19C=	ENSP00000329546.3:n.250+19C=
ENST00000375581.3:c.316+19C=	ENSP00000364731.3:n.316+19C=
ENST00000444337.1:c.*7C=	ENSP00000387669.1:n.*7C=
ENST00000473085.1:n.197+19C=
ENST00000479674.1:n.532C=
ENST00000541084.5:c.65-52C=	ENSP00000442051.2:n.65-52C=
NM_000131.4:c.316+19C= , LRG_554t1:c.316+19C=	NP_000122.1:n.316+19C=
NM_001267554.1:c.65-52C=	NP_001254483.1:n.65-52C=
NM_019616.3:c.250+19C= , LRG_554t2:c.250+19C=	NP_062562.1:n.250+19C=
NR_051961.1:n.286C=
XM_006719963.2:c.250+19C=	XP_006720026.1:n.250+19C=
XM_011537474.1:c.250+19C=	XP_011535776.1:n.250+19C=
XM_011537475.1:c.65-52C=	XP_011535777.1:n.65-52C=
XM_011537477.1:c.212-52C=	XP_011535779.1:n.212-52C=
XM_006719963.3:c.295+19C=	XP_006720026.2:n.295+19C=
XM_011537474.2:c.295+19C=	XP_011535776.2:n.295+19C=
XM_011537475.2:c.110-52C=	XP_011535777.2:n.110-52C=
NM_019616.4:c.250+19C= MANE Select	NP_062562.1:n.250+19C=
NR_051961.2:n.283C=
NM_001267554.2:c.65-52C=	NP_001254483.1:n.65-52C=