Canonical Allele Identifier: CA388786485

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773077T>G (hg19) ; chr13:g.113118763T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118763T>G , CM000675.2:g.113118763T>G	GRCh38
NC_000013.10:g.113773077T>G , CM000675.1:g.113773077T>G	GRCh37
NC_000013.9:g.112821078T>G	NCBI36
NG_009258.1:g.965T>G , LRG_548:g.965T>G
NG_009262.1:g.17973T>G , LRG_554:g.17973T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1090T>G MANE Select	ENSP00000329546.4:p.Tyr364Asp
ENST00000346342.7:c.1090T>G	ENSP00000329546.3:p.Tyr364Asp
ENST00000375581.3:c.1156T>G	ENSP00000364731.3:p.Tyr386Asp
ENST00000541084.5:c.904T>G	ENSP00000442051.2:p.Tyr302Asp
NM_000131.4:c.1156T>G , LRG_554t1:c.1156T>G	NP_000122.1:p.Tyr386Asp
NM_001267554.1:c.904T>G	NP_001254483.1:p.Tyr302Asp
NM_019616.3:c.1090T>G , LRG_554t2:c.1090T>G	NP_062562.1:p.Tyr364Asp
NR_051961.1:n.1177T>G
XM_006719963.2:c.949T>G	XP_006720026.1:p.Tyr317Asp
XM_011537474.1:c.1198T>G	XP_011535776.1:p.Tyr400Asp
XM_011537475.1:c.1012T>G	XP_011535777.1:p.Tyr338Asp
XM_011537476.1:c.850T>G	XP_011535778.1:p.Tyr284Asp
XM_011537477.1:c.1159T>G	XP_011535779.1:p.Tyr387Asp
XM_006719963.3:c.994T>G	XP_006720026.2:p.Tyr332Asp
XM_011537474.2:c.1243T>G	XP_011535776.2:p.Tyr415Asp
XM_011537475.2:c.1057T>G	XP_011535777.2:p.Tyr353Asp
XM_011537476.2:c.850T>G	XP_011535778.1:p.Tyr284Asp
NM_019616.4:c.1090T>G MANE Select	NP_062562.1:p.Tyr364Asp
NR_051961.2:n.1174T>G
NM_001267554.2:c.904T>G	NP_001254483.1:p.Tyr302Asp