Canonical Allele Identifier: CA388782513

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768265T>C (hg19) ; chr13:g.113113951T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113951T>C , CM000675.2:g.113113951T>C	GRCh38
NC_000013.10:g.113768265T>C , CM000675.1:g.113768265T>C	GRCh37
NC_000013.9:g.112816266T>C	NCBI36
NG_009262.1:g.13161T>C , LRG_554:g.13161T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.355T>C MANE Select	ENSP00000329546.4:p.Cys119Arg
ENST00000346342.7:c.355T>C	ENSP00000329546.3:p.Cys119Arg
ENST00000375581.3:c.421T>C	ENSP00000364731.3:p.Cys141Arg
ENST00000444337.1:c.*163T>C	ENSP00000387669.1:n.*163T>C
ENST00000473085.1:n.302T>C
ENST00000479674.1:n.688T>C
ENST00000541084.5:c.169T>C	ENSP00000442051.2:p.Cys57Arg
NM_000131.4:c.421T>C , LRG_554t1:c.421T>C	NP_000122.1:p.Cys141Arg
NM_001267554.1:c.169T>C	NP_001254483.1:p.Cys57Arg
NM_019616.3:c.355T>C , LRG_554t2:c.355T>C	NP_062562.1:p.Cys119Arg
NR_051961.1:n.442T>C
XM_006719963.2:c.355T>C	XP_006720026.1:p.Cys119Arg
XM_011537474.1:c.355T>C	XP_011535776.1:p.Cys119Arg
XM_011537475.1:c.169T>C	XP_011535777.1:p.Cys57Arg
XM_011537477.1:c.316T>C	XP_011535779.1:p.Cys106Arg
XM_006719963.3:c.400T>C	XP_006720026.2:p.Cys134Arg
XM_011537474.2:c.400T>C	XP_011535776.2:p.Cys134Arg
XM_011537475.2:c.214T>C	XP_011535777.2:p.Cys72Arg
NM_019616.4:c.355T>C MANE Select	NP_062562.1:p.Cys119Arg
NR_051961.2:n.439T>C
NM_001267554.2:c.169T>C	NP_001254483.1:p.Cys57Arg