Canonical Allele Identifier: CA485423861

Gene: F7

Linked Data

• gnomAD v4: 13-113118498-C-T
• MyVariant Identifiers: chr13:g.113772812C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118498C>T , CM000675.2:g.113118498C>T	GRCh38
NC_000013.10:g.113772812C>T , CM000675.1:g.113772812C>T	GRCh37
NC_000013.9:g.112820813C>T	NCBI36
NG_009258.1:g.700C>T , LRG_548:g.700C>T
NG_009262.1:g.17708C>T , LRG_554:g.17708C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.825C>T MANE Select	ENSP00000329546.4:p.Gly275=
ENST00000346342.7:c.825C>T	ENSP00000329546.3:p.Gly275=
ENST00000375581.3:c.891C>T	ENSP00000364731.3:p.Gly297=
ENST00000541084.5:c.639C>T	ENSP00000442051.2:p.Gly213=
NM_000131.4:c.891C>T , LRG_554t1:c.891C>T	NP_000122.1:p.Gly297=
NM_001267554.1:c.639C>T	NP_001254483.1:p.Gly213=
NM_019616.3:c.825C>T , LRG_554t2:c.825C>T	NP_062562.1:p.Gly275=
NR_051961.1:n.912C>T
XM_006719963.2:c.684C>T	XP_006720026.1:p.Gly228=
XM_011537474.1:c.933C>T	XP_011535776.1:p.Gly311=
XM_011537475.1:c.747C>T	XP_011535777.1:p.Gly249=
XM_011537476.1:c.585C>T	XP_011535778.1:p.Gly195=
XM_011537477.1:c.894C>T	XP_011535779.1:p.Gly298=
XM_006719963.3:c.729C>T	XP_006720026.2:p.Gly243=
XM_011537474.2:c.978C>T	XP_011535776.2:p.Gly326=
XM_011537475.2:c.792C>T	XP_011535777.2:p.Gly264=
XM_011537476.2:c.585C>T	XP_011535778.1:p.Gly195=
NM_019616.4:c.825C>T MANE Select	NP_062562.1:p.Gly275=
NR_051961.2:n.909C>T
NM_001267554.2:c.639C>T	NP_001254483.1:p.Gly213=