Canonical Allele Identifier: CA485423852

Gene: F7

Linked Data

• gnomAD v4: 13-113118483-C-T
• MyVariant Identifiers: chr13:g.113772797C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118483C>T , CM000675.2:g.113118483C>T	GRCh38
NC_000013.10:g.113772797C>T , CM000675.1:g.113772797C>T	GRCh37
NC_000013.9:g.112820798C>T	NCBI36
NG_009258.1:g.685C>T , LRG_548:g.685C>T
NG_009262.1:g.17693C>T , LRG_554:g.17693C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.810C>T MANE Select	ENSP00000329546.4:p.Ser270=
ENST00000346342.7:c.810C>T	ENSP00000329546.3:p.Ser270=
ENST00000375581.3:c.876C>T	ENSP00000364731.3:p.Ser292=
ENST00000541084.5:c.624C>T	ENSP00000442051.2:p.Ser208=
NM_000131.4:c.876C>T , LRG_554t1:c.876C>T	NP_000122.1:p.Ser292=
NM_001267554.1:c.624C>T	NP_001254483.1:p.Ser208=
NM_019616.3:c.810C>T , LRG_554t2:c.810C>T	NP_062562.1:p.Ser270=
NR_051961.1:n.897C>T
XM_006719963.2:c.669C>T	XP_006720026.1:p.Ser223=
XM_011537474.1:c.918C>T	XP_011535776.1:p.Ser306=
XM_011537475.1:c.732C>T	XP_011535777.1:p.Ser244=
XM_011537476.1:c.570C>T	XP_011535778.1:p.Ser190=
XM_011537477.1:c.879C>T	XP_011535779.1:p.Ser293=
XM_006719963.3:c.714C>T	XP_006720026.2:p.Ser238=
XM_011537474.2:c.963C>T	XP_011535776.2:p.Ser321=
XM_011537475.2:c.777C>T	XP_011535777.2:p.Ser259=
XM_011537476.2:c.570C>T	XP_011535778.1:p.Ser190=
NM_019616.4:c.810C>T MANE Select	NP_062562.1:p.Ser270=
NR_051961.2:n.894C>T
NM_001267554.2:c.624C>T	NP_001254483.1:p.Ser208=