Canonical Allele Identifier: CA388785921

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772805T>G (hg19) ; chr13:g.113118491T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118491T>G , CM000675.2:g.113118491T>G	GRCh38
NC_000013.10:g.113772805T>G , CM000675.1:g.113772805T>G	GRCh37
NC_000013.9:g.112820806T>G	NCBI36
NG_009258.1:g.693T>G , LRG_548:g.693T>G
NG_009262.1:g.17701T>G , LRG_554:g.17701T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.818T>G MANE Select	ENSP00000329546.4:p.Val273Gly
ENST00000346342.7:c.818T>G	ENSP00000329546.3:p.Val273Gly
ENST00000375581.3:c.884T>G	ENSP00000364731.3:p.Val295Gly
ENST00000541084.5:c.632T>G	ENSP00000442051.2:p.Val211Gly
NM_000131.4:c.884T>G , LRG_554t1:c.884T>G	NP_000122.1:p.Val295Gly
NM_001267554.1:c.632T>G	NP_001254483.1:p.Val211Gly
NM_019616.3:c.818T>G , LRG_554t2:c.818T>G	NP_062562.1:p.Val273Gly
NR_051961.1:n.905T>G
XM_006719963.2:c.677T>G	XP_006720026.1:p.Val226Gly
XM_011537474.1:c.926T>G	XP_011535776.1:p.Val309Gly
XM_011537475.1:c.740T>G	XP_011535777.1:p.Val247Gly
XM_011537476.1:c.578T>G	XP_011535778.1:p.Val193Gly
XM_011537477.1:c.887T>G	XP_011535779.1:p.Val296Gly
XM_006719963.3:c.722T>G	XP_006720026.2:p.Val241Gly
XM_011537474.2:c.971T>G	XP_011535776.2:p.Val324Gly
XM_011537475.2:c.785T>G	XP_011535777.2:p.Val262Gly
XM_011537476.2:c.578T>G	XP_011535778.1:p.Val193Gly
NM_019616.4:c.818T>G MANE Select	NP_062562.1:p.Val273Gly
NR_051961.2:n.902T>G
NM_001267554.2:c.632T>G	NP_001254483.1:p.Val211Gly