Canonical Allele Identifier: CA388787154

Gene: F7

Linked Data

• gnomAD v4: 13-113118958-A-G
• MyVariant Identifiers: chr13:g.113773272A>G (hg19) ; chr13:g.113118958A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118958A>G , CM000675.2:g.113118958A>G	GRCh38
NC_000013.10:g.113773272A>G , CM000675.1:g.113773272A>G	GRCh37
NC_000013.9:g.112821273A>G	NCBI36
NG_009258.1:g.1160A>G , LRG_548:g.1160A>G
NG_009262.1:g.18168A>G , LRG_554:g.18168A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1285A>G MANE Select	ENSP00000329546.4:p.Met429Val
ENST00000346342.7:c.1285A>G	ENSP00000329546.3:p.Met429Val
ENST00000375581.3:c.1351A>G	ENSP00000364731.3:p.Met451Val
ENST00000541084.5:c.1099A>G	ENSP00000442051.2:p.Met367Val
NM_000131.4:c.1351A>G , LRG_554t1:c.1351A>G	NP_000122.1:p.Met451Val
NM_001267554.1:c.1099A>G	NP_001254483.1:p.Met367Val
NM_019616.3:c.1285A>G , LRG_554t2:c.1285A>G	NP_062562.1:p.Met429Val
NR_051961.1:n.1372A>G
XM_006719963.2:c.1144A>G	XP_006720026.1:p.Met382Val
XM_011537474.1:c.1393A>G	XP_011535776.1:p.Met465Val
XM_011537475.1:c.1207A>G	XP_011535777.1:p.Met403Val
XM_011537476.1:c.1045A>G	XP_011535778.1:p.Met349Val
XM_011537477.1:c.1354A>G	XP_011535779.1:p.Met452Val
XM_006719963.3:c.1189A>G	XP_006720026.2:p.Met397Val
XM_011537474.2:c.1438A>G	XP_011535776.2:p.Met480Val
XM_011537475.2:c.1252A>G	XP_011535777.2:p.Met418Val
XM_011537476.2:c.1045A>G	XP_011535778.1:p.Met349Val
NM_019616.4:c.1285A>G MANE Select	NP_062562.1:p.Met429Val
NR_051961.2:n.1369A>G
NM_001267554.2:c.1099A>G	NP_001254483.1:p.Met367Val