Canonical Allele Identifier: CA388785824

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772756G>C (hg19) ; chr13:g.113118442G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118442G>C , CM000675.2:g.113118442G>C	GRCh38
NC_000013.10:g.113772756G>C , CM000675.1:g.113772756G>C	GRCh37
NC_000013.9:g.112820757G>C	NCBI36
NG_009258.1:g.644G>C , LRG_548:g.644G>C
NG_009262.1:g.17652G>C , LRG_554:g.17652G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.769G>C MANE Select	ENSP00000329546.4:p.Asp257His
ENST00000346342.7:c.769G>C	ENSP00000329546.3:p.Asp257His
ENST00000375581.3:c.835G>C	ENSP00000364731.3:p.Asp279His
ENST00000541084.5:c.583G>C	ENSP00000442051.2:p.Asp195His
NM_000131.4:c.835G>C , LRG_554t1:c.835G>C	NP_000122.1:p.Asp279His
NM_001267554.1:c.583G>C	NP_001254483.1:p.Asp195His
NM_019616.3:c.769G>C , LRG_554t2:c.769G>C	NP_062562.1:p.Asp257His
NR_051961.1:n.856G>C
XM_006719963.2:c.628G>C	XP_006720026.1:p.Asp210His
XM_011537474.1:c.877G>C	XP_011535776.1:p.Asp293His
XM_011537475.1:c.691G>C	XP_011535777.1:p.Asp231His
XM_011537476.1:c.529G>C	XP_011535778.1:p.Asp177His
XM_011537477.1:c.838G>C	XP_011535779.1:p.Asp280His
XM_006719963.3:c.673G>C	XP_006720026.2:p.Asp225His
XM_011537474.2:c.922G>C	XP_011535776.2:p.Asp308His
XM_011537475.2:c.736G>C	XP_011535777.2:p.Asp246His
XM_011537476.2:c.529G>C	XP_011535778.1:p.Asp177His
NM_019616.4:c.769G>C MANE Select	NP_062562.1:p.Asp257His
NR_051961.2:n.853G>C
NM_001267554.2:c.583G>C	NP_001254483.1:p.Asp195His