Canonical Allele Identifier: CA7059796

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113105812A>C , CM000675.2:g.113105812A>C	GRCh38
NC_000013.10:g.113760126A>C , CM000675.1:g.113760126A>C	GRCh37
NC_000013.9:g.112808127A>C	NCBI36
NG_009262.1:g.5022A>C , LRG_554:g.5022A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.-30A>C MANE Select	NP_062562.1:n.-30A>C
ENST00000346342.8:c.-30A>C MANE Select	ENSP00000329546.4:n.-30A>C
NM_000131.4:c.-30A>C , LRG_554t1:c.-30A>C	NP_000122.1:n.-30A>C
NM_001267554.1:c.-30A>C	NP_001254483.1:n.-30A>C
NM_001267554.2:c.-30A>C	NP_001254483.1:n.-30A>C
NM_019616.3:c.-30A>C , LRG_554t2:c.-30A>C	NP_062562.1:n.-30A>C
NR_051961.1:n.25A>C
NR_051961.2:n.22A>C
ENST00000346342.7:c.-30A>C	ENSP00000329546.3:n.-30A>C
ENST00000375581.3:c.-30A>C	ENSP00000364731.3:n.-30A>C
ENST00000541084.5:c.-30A>C	ENSP00000442051.2:n.-30A>C
XM_006719963.3:c.16A>C	XP_006720026.2:p.Arg6=
XM_011537474.2:c.16A>C	XP_011535776.2:p.Arg6=
XM_011537475.2:c.16A>C	XP_011535777.2:p.Arg6=
XM_011537477.1:c.-30A>C	XP_011535779.1:n.-30A>C