Canonical Allele Identifier: CA388786146

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772922C>A (hg19) ; chr13:g.113118608C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118608C>A , CM000675.2:g.113118608C>A	GRCh38
NC_000013.10:g.113772922C>A , CM000675.1:g.113772922C>A	GRCh37
NC_000013.9:g.112820923C>A	NCBI36
NG_009258.1:g.810C>A , LRG_548:g.810C>A
NG_009262.1:g.17818C>A , LRG_554:g.17818C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.935C>A MANE Select	ENSP00000329546.4:p.Ala312Asp
ENST00000346342.7:c.935C>A	ENSP00000329546.3:p.Ala312Asp
ENST00000375581.3:c.1001C>A	ENSP00000364731.3:p.Ala334Asp
ENST00000541084.5:c.749C>A	ENSP00000442051.2:p.Ala250Asp
NM_000131.4:c.1001C>A , LRG_554t1:c.1001C>A	NP_000122.1:p.Ala334Asp
NM_001267554.1:c.749C>A	NP_001254483.1:p.Ala250Asp
NM_019616.3:c.935C>A , LRG_554t2:c.935C>A	NP_062562.1:p.Ala312Asp
NR_051961.1:n.1022C>A
XM_006719963.2:c.794C>A	XP_006720026.1:p.Ala265Asp
XM_011537474.1:c.1043C>A	XP_011535776.1:p.Ala348Asp
XM_011537475.1:c.857C>A	XP_011535777.1:p.Ala286Asp
XM_011537476.1:c.695C>A	XP_011535778.1:p.Ala232Asp
XM_011537477.1:c.1004C>A	XP_011535779.1:p.Ala335Asp
XM_006719963.3:c.839C>A	XP_006720026.2:p.Ala280Asp
XM_011537474.2:c.1088C>A	XP_011535776.2:p.Ala363Asp
XM_011537475.2:c.902C>A	XP_011535777.2:p.Ala301Asp
XM_011537476.2:c.695C>A	XP_011535778.1:p.Ala232Asp
NM_019616.4:c.935C>A MANE Select	NP_062562.1:p.Ala312Asp
NR_051961.2:n.1019C>A
NM_001267554.2:c.749C>A	NP_001254483.1:p.Ala250Asp