Canonical Allele Identifier: CA388787219

Gene: F7

Linked Data

• gnomAD v4: 13-113118995-C-A
• MyVariant Identifiers: chr13:g.113773309C>A (hg19) ; chr13:g.113118995C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118995C>A , CM000675.2:g.113118995C>A	GRCh38
NC_000013.10:g.113773309C>A , CM000675.1:g.113773309C>A	GRCh37
NC_000013.9:g.112821310C>A	NCBI36
NG_009258.1:g.1197C>A , LRG_548:g.1197C>A
NG_009262.1:g.18205C>A , LRG_554:g.18205C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1322C>A MANE Select	ENSP00000329546.4:p.Ala441Asp
ENST00000346342.7:c.1322C>A	ENSP00000329546.3:p.Ala441Asp
ENST00000375581.3:c.1388C>A	ENSP00000364731.3:p.Ala463Asp
ENST00000541084.5:c.1136C>A	ENSP00000442051.2:p.Ala379Asp
NM_000131.4:c.1388C>A , LRG_554t1:c.1388C>A	NP_000122.1:p.Ala463Asp
NM_001267554.1:c.1136C>A	NP_001254483.1:p.Ala379Asp
NM_019616.3:c.1322C>A , LRG_554t2:c.1322C>A	NP_062562.1:p.Ala441Asp
NR_051961.1:n.1409C>A
XM_006719963.2:c.1181C>A	XP_006720026.1:p.Ala394Asp
XM_011537474.1:c.1430C>A	XP_011535776.1:p.Ala477Asp
XM_011537475.1:c.1244C>A	XP_011535777.1:p.Ala415Asp
XM_011537476.1:c.1082C>A	XP_011535778.1:p.Ala361Asp
XM_011537477.1:c.1391C>A	XP_011535779.1:p.Ala464Asp
XM_006719963.3:c.1226C>A	XP_006720026.2:p.Ala409Asp
XM_011537474.2:c.1475C>A	XP_011535776.2:p.Ala492Asp
XM_011537475.2:c.1289C>A	XP_011535777.2:p.Ala430Asp
XM_011537476.2:c.1082C>A	XP_011535778.1:p.Ala361Asp
NM_019616.4:c.1322C>A MANE Select	NP_062562.1:p.Ala441Asp
NR_051961.2:n.1406C>A
NM_001267554.2:c.1136C>A	NP_001254483.1:p.Ala379Asp