Canonical Allele Identifier: CA388782415

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113768242T>C (hg19) ; chr13:g.113113928T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113928T>C , CM000675.2:g.113113928T>C	GRCh38
NC_000013.10:g.113768242T>C , CM000675.1:g.113768242T>C	GRCh37
NC_000013.9:g.112816243T>C	NCBI36
NG_009262.1:g.13138T>C , LRG_554:g.13138T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.332T>C MANE Select	ENSP00000329546.4:p.Leu111Pro
ENST00000346342.7:c.332T>C	ENSP00000329546.3:p.Leu111Pro
ENST00000375581.3:c.398T>C	ENSP00000364731.3:p.Leu133Pro
ENST00000444337.1:c.*140T>C	ENSP00000387669.1:n.*140T>C
ENST00000473085.1:n.279T>C
ENST00000479674.1:n.665T>C
ENST00000541084.5:c.146T>C	ENSP00000442051.2:p.Leu49Pro
NM_000131.4:c.398T>C , LRG_554t1:c.398T>C	NP_000122.1:p.Leu133Pro
NM_001267554.1:c.146T>C	NP_001254483.1:p.Leu49Pro
NM_019616.3:c.332T>C , LRG_554t2:c.332T>C	NP_062562.1:p.Leu111Pro
NR_051961.1:n.419T>C
XM_006719963.2:c.332T>C	XP_006720026.1:p.Leu111Pro
XM_011537474.1:c.332T>C	XP_011535776.1:p.Leu111Pro
XM_011537475.1:c.146T>C	XP_011535777.1:p.Leu49Pro
XM_011537477.1:c.293T>C	XP_011535779.1:p.Leu98Pro
XM_006719963.3:c.377T>C	XP_006720026.2:p.Leu126Pro
XM_011537474.2:c.377T>C	XP_011535776.2:p.Leu126Pro
XM_011537475.2:c.191T>C	XP_011535777.2:p.Leu64Pro
NM_019616.4:c.332T>C MANE Select	NP_062562.1:p.Leu111Pro
NR_051961.2:n.416T>C
NM_001267554.2:c.146T>C	NP_001254483.1:p.Leu49Pro