Canonical Allele Identifier: CA388782522

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768266G>T (hg19) ; chr13:g.113113952G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113952G>T , CM000675.2:g.113113952G>T	GRCh38
NC_000013.10:g.113768266G>T , CM000675.1:g.113768266G>T	GRCh37
NC_000013.9:g.112816267G>T	NCBI36
NG_009262.1:g.13162G>T , LRG_554:g.13162G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.356G>T MANE Select	ENSP00000329546.4:p.Cys119Phe
ENST00000346342.7:c.356G>T	ENSP00000329546.3:p.Cys119Phe
ENST00000375581.3:c.422G>T	ENSP00000364731.3:p.Cys141Phe
ENST00000444337.1:c.*164G>T	ENSP00000387669.1:n.*164G>T
ENST00000473085.1:n.303G>T
ENST00000479674.1:n.689G>T
ENST00000541084.5:c.170G>T	ENSP00000442051.2:p.Cys57Phe
NM_000131.4:c.422G>T , LRG_554t1:c.422G>T	NP_000122.1:p.Cys141Phe
NM_001267554.1:c.170G>T	NP_001254483.1:p.Cys57Phe
NM_019616.3:c.356G>T , LRG_554t2:c.356G>T	NP_062562.1:p.Cys119Phe
NR_051961.1:n.443G>T
XM_006719963.2:c.356G>T	XP_006720026.1:p.Cys119Phe
XM_011537474.1:c.356G>T	XP_011535776.1:p.Cys119Phe
XM_011537475.1:c.170G>T	XP_011535777.1:p.Cys57Phe
XM_011537477.1:c.317G>T	XP_011535779.1:p.Cys106Phe
XM_006719963.3:c.401G>T	XP_006720026.2:p.Cys134Phe
XM_011537474.2:c.401G>T	XP_011535776.2:p.Cys134Phe
XM_011537475.2:c.215G>T	XP_011535777.2:p.Cys72Phe
NM_019616.4:c.356G>T MANE Select	NP_062562.1:p.Cys119Phe
NR_051961.2:n.440G>T
NM_001267554.2:c.170G>T	NP_001254483.1:p.Cys57Phe