Canonical Allele Identifier: CA388786792

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773143C>G (hg19) ; chr13:g.113118829C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118829C>G , CM000675.2:g.113118829C>G	GRCh38
NC_000013.10:g.113773143C>G , CM000675.1:g.113773143C>G	GRCh37
NC_000013.9:g.112821144C>G	NCBI36
NG_009258.1:g.1031C>G , LRG_548:g.1031C>G
NG_009262.1:g.18039C>G , LRG_554:g.18039C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1156C>G MANE Select	ENSP00000329546.4:p.His386Asp
ENST00000346342.7:c.1156C>G	ENSP00000329546.3:p.His386Asp
ENST00000375581.3:c.1222C>G	ENSP00000364731.3:p.His408Asp
ENST00000541084.5:c.970C>G	ENSP00000442051.2:p.His324Asp
NM_000131.4:c.1222C>G , LRG_554t1:c.1222C>G	NP_000122.1:p.His408Asp
NM_001267554.1:c.970C>G	NP_001254483.1:p.His324Asp
NM_019616.3:c.1156C>G , LRG_554t2:c.1156C>G	NP_062562.1:p.His386Asp
NR_051961.1:n.1243C>G
XM_006719963.2:c.1015C>G	XP_006720026.1:p.His339Asp
XM_011537474.1:c.1264C>G	XP_011535776.1:p.His422Asp
XM_011537475.1:c.1078C>G	XP_011535777.1:p.His360Asp
XM_011537476.1:c.916C>G	XP_011535778.1:p.His306Asp
XM_011537477.1:c.1225C>G	XP_011535779.1:p.His409Asp
XM_006719963.3:c.1060C>G	XP_006720026.2:p.His354Asp
XM_011537474.2:c.1309C>G	XP_011535776.2:p.His437Asp
XM_011537475.2:c.1123C>G	XP_011535777.2:p.His375Asp
XM_011537476.2:c.916C>G	XP_011535778.1:p.His306Asp
NM_019616.4:c.1156C>G MANE Select	NP_062562.1:p.His386Asp
NR_051961.2:n.1240C>G
NM_001267554.2:c.970C>G	NP_001254483.1:p.His324Asp