Canonical Allele Identifier: CA388786730

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773129A>G (hg19) ; chr13:g.113118815A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118815A>G , CM000675.2:g.113118815A>G	GRCh38
NC_000013.10:g.113773129A>G , CM000675.1:g.113773129A>G	GRCh37
NC_000013.9:g.112821130A>G	NCBI36
NG_009258.1:g.1017A>G , LRG_548:g.1017A>G
NG_009262.1:g.18025A>G , LRG_554:g.18025A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1142A>G MANE Select	ENSP00000329546.4:p.Asp381Gly
ENST00000346342.7:c.1142A>G	ENSP00000329546.3:p.Asp381Gly
ENST00000375581.3:c.1208A>G	ENSP00000364731.3:p.Asp403Gly
ENST00000541084.5:c.956A>G	ENSP00000442051.2:p.Asp319Gly
NM_000131.4:c.1208A>G , LRG_554t1:c.1208A>G	NP_000122.1:p.Asp403Gly
NM_001267554.1:c.956A>G	NP_001254483.1:p.Asp319Gly
NM_019616.3:c.1142A>G , LRG_554t2:c.1142A>G	NP_062562.1:p.Asp381Gly
NR_051961.1:n.1229A>G
XM_006719963.2:c.1001A>G	XP_006720026.1:p.Asp334Gly
XM_011537474.1:c.1250A>G	XP_011535776.1:p.Asp417Gly
XM_011537475.1:c.1064A>G	XP_011535777.1:p.Asp355Gly
XM_011537476.1:c.902A>G	XP_011535778.1:p.Asp301Gly
XM_011537477.1:c.1211A>G	XP_011535779.1:p.Asp404Gly
XM_006719963.3:c.1046A>G	XP_006720026.2:p.Asp349Gly
XM_011537474.2:c.1295A>G	XP_011535776.2:p.Asp432Gly
XM_011537475.2:c.1109A>G	XP_011535777.2:p.Asp370Gly
XM_011537476.2:c.902A>G	XP_011535778.1:p.Asp301Gly
NM_019616.4:c.1142A>G MANE Select	NP_062562.1:p.Asp381Gly
NR_051961.2:n.1226A>G
NM_001267554.2:c.956A>G	NP_001254483.1:p.Asp319Gly