Canonical Allele Identifier: CA256461976

Gene: F7

Linked Data

• dbSNP Id: rs987619098
• gnomAD v3: 13-113118994-G-A
• gnomAD v4: 13-113118994-G-A
• MyVariant Identifiers: chr13:g.113773308G>A (hg19) ; chr13:g.113118994G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118994G>A , CM000675.2:g.113118994G>A	GRCh38
NC_000013.10:g.113773308G>A , CM000675.1:g.113773308G>A	GRCh37
NC_000013.9:g.112821309G>A	NCBI36
NG_009258.1:g.1196G>A , LRG_548:g.1196G>A
NG_009262.1:g.18204G>A , LRG_554:g.18204G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1321G>A MANE Select	ENSP00000329546.4:p.Ala441Thr
ENST00000346342.7:c.1321G>A	ENSP00000329546.3:p.Ala441Thr
ENST00000375581.3:c.1387G>A	ENSP00000364731.3:p.Ala463Thr
ENST00000541084.5:c.1135G>A	ENSP00000442051.2:p.Ala379Thr
NM_000131.4:c.1387G>A , LRG_554t1:c.1387G>A	NP_000122.1:p.Ala463Thr
NM_001267554.1:c.1135G>A	NP_001254483.1:p.Ala379Thr
NM_019616.3:c.1321G>A , LRG_554t2:c.1321G>A	NP_062562.1:p.Ala441Thr
NR_051961.1:n.1408G>A
XM_006719963.2:c.1180G>A	XP_006720026.1:p.Ala394Thr
XM_011537474.1:c.1429G>A	XP_011535776.1:p.Ala477Thr
XM_011537475.1:c.1243G>A	XP_011535777.1:p.Ala415Thr
XM_011537476.1:c.1081G>A	XP_011535778.1:p.Ala361Thr
XM_011537477.1:c.1390G>A	XP_011535779.1:p.Ala464Thr
XM_006719963.3:c.1225G>A	XP_006720026.2:p.Ala409Thr
XM_011537474.2:c.1474G>A	XP_011535776.2:p.Ala492Thr
XM_011537475.2:c.1288G>A	XP_011535777.2:p.Ala430Thr
XM_011537476.2:c.1081G>A	XP_011535778.1:p.Ala361Thr
NM_019616.4:c.1321G>A MANE Select	NP_062562.1:p.Ala441Thr
NR_051961.2:n.1405G>A
NM_001267554.2:c.1135G>A	NP_001254483.1:p.Ala379Thr