Canonical Allele Identifier: CA2623810949

Gene: F7

Linked Data

• gnomAD v4: 13-113119594-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113119594G>T , CM000675.2:g.113119594G>T	GRCh38
NC_000013.10:g.113773908G>T , CM000675.1:g.113773908G>T	GRCh37
NC_000013.9:g.112821909G>T	NCBI36
NG_009258.1:g.1796G>T , LRG_548:g.1796G>T
NG_009262.1:g.18804G>T , LRG_554:g.18804G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.*586G>T MANE Select	ENSP00000329546.4:n.*586G>T
ENST00000346342.7:c.*586G>T	ENSP00000329546.3:n.*586G>T
ENST00000375581.3:c.*586G>T	ENSP00000364731.3:n.*586G>T
ENST00000541084.5:c.*586G>T	ENSP00000442051.2:n.*586G>T
NM_000131.4:c.*586G>T , LRG_554t1:c.*586G>T	NP_000122.1:n.*586G>T
NM_001267554.1:c.*586G>T	NP_001254483.1:n.*586G>T
NM_019616.3:c.*586G>T , LRG_554t2:c.*586G>T	NP_062562.1:n.*586G>T
NR_051961.1:n.2008G>T
XM_006719963.2:c.*586G>T	XP_006720026.1:n.*586G>T
XM_011537474.1:c.*586G>T	XP_011535776.1:n.*586G>T
XM_011537475.1:c.*586G>T	XP_011535777.1:n.*586G>T
XM_011537476.1:c.*586G>T	XP_011535778.1:n.*586G>T
XM_011537477.1:c.*586G>T	XP_011535779.1:n.*586G>T
XM_006719963.3:c.*586G>T	XP_006720026.2:n.*586G>T
XM_011537474.2:c.*586G>T	XP_011535776.2:n.*586G>T
XM_011537475.2:c.*586G>T	XP_011535777.2:n.*586G>T
XM_011537476.2:c.*586G>T	XP_011535778.1:n.*586G>T
NM_019616.4:c.*586G>T MANE Select	NP_062562.1:n.*586G>T
NR_051961.2:n.2005G>T
NM_001267554.2:c.*586G>T	NP_001254483.1:n.*586G>T