Canonical Allele Identifier: CA388785837

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772761G>C (hg19) ; chr13:g.113118447G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118447G>C , CM000675.2:g.113118447G>C	GRCh38
NC_000013.10:g.113772761G>C , CM000675.1:g.113772761G>C	GRCh37
NC_000013.9:g.112820762G>C	NCBI36
NG_009258.1:g.649G>C , LRG_548:g.649G>C
NG_009262.1:g.17657G>C , LRG_554:g.17657G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.774G>C MANE Select	ENSP00000329546.4:p.Glu258Asp
ENST00000346342.7:c.774G>C	ENSP00000329546.3:p.Glu258Asp
ENST00000375581.3:c.840G>C	ENSP00000364731.3:p.Glu280Asp
ENST00000541084.5:c.588G>C	ENSP00000442051.2:p.Glu196Asp
NM_000131.4:c.840G>C , LRG_554t1:c.840G>C	NP_000122.1:p.Glu280Asp
NM_001267554.1:c.588G>C	NP_001254483.1:p.Glu196Asp
NM_019616.3:c.774G>C , LRG_554t2:c.774G>C	NP_062562.1:p.Glu258Asp
NR_051961.1:n.861G>C
XM_006719963.2:c.633G>C	XP_006720026.1:p.Glu211Asp
XM_011537474.1:c.882G>C	XP_011535776.1:p.Glu294Asp
XM_011537475.1:c.696G>C	XP_011535777.1:p.Glu232Asp
XM_011537476.1:c.534G>C	XP_011535778.1:p.Glu178Asp
XM_011537477.1:c.843G>C	XP_011535779.1:p.Glu281Asp
XM_006719963.3:c.678G>C	XP_006720026.2:p.Glu226Asp
XM_011537474.2:c.927G>C	XP_011535776.2:p.Glu309Asp
XM_011537475.2:c.741G>C	XP_011535777.2:p.Glu247Asp
XM_011537476.2:c.534G>C	XP_011535778.1:p.Glu178Asp
NM_019616.4:c.774G>C MANE Select	NP_062562.1:p.Glu258Asp
NR_051961.2:n.858G>C
NM_001267554.2:c.588G>C	NP_001254483.1:p.Glu196Asp