Canonical Allele Identifier: CA388786263

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772981G>A (hg19) ; chr13:g.113118667G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118667G>A , CM000675.2:g.113118667G>A	GRCh38
NC_000013.10:g.113772981G>A , CM000675.1:g.113772981G>A	GRCh37
NC_000013.9:g.112820982G>A	NCBI36
NG_009258.1:g.869G>A , LRG_548:g.869G>A
NG_009262.1:g.17877G>A , LRG_554:g.17877G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.994G>A MANE Select	ENSP00000329546.4:p.Ala332Thr
ENST00000346342.7:c.994G>A	ENSP00000329546.3:p.Ala332Thr
ENST00000375581.3:c.1060G>A	ENSP00000364731.3:p.Ala354Thr
ENST00000541084.5:c.808G>A	ENSP00000442051.2:p.Ala270Thr
NM_000131.4:c.1060G>A , LRG_554t1:c.1060G>A	NP_000122.1:p.Ala354Thr
NM_001267554.1:c.808G>A	NP_001254483.1:p.Ala270Thr
NM_019616.3:c.994G>A , LRG_554t2:c.994G>A	NP_062562.1:p.Ala332Thr
NR_051961.1:n.1081G>A
XM_006719963.2:c.853G>A	XP_006720026.1:p.Ala285Thr
XM_011537474.1:c.1102G>A	XP_011535776.1:p.Ala368Thr
XM_011537475.1:c.916G>A	XP_011535777.1:p.Ala306Thr
XM_011537476.1:c.754G>A	XP_011535778.1:p.Ala252Thr
XM_011537477.1:c.1063G>A	XP_011535779.1:p.Ala355Thr
XM_006719963.3:c.898G>A	XP_006720026.2:p.Ala300Thr
XM_011537474.2:c.1147G>A	XP_011535776.2:p.Ala383Thr
XM_011537475.2:c.961G>A	XP_011535777.2:p.Ala321Thr
XM_011537476.2:c.754G>A	XP_011535778.1:p.Ala252Thr
NM_019616.4:c.994G>A MANE Select	NP_062562.1:p.Ala332Thr
NR_051961.2:n.1078G>A
NM_001267554.2:c.808G>A	NP_001254483.1:p.Ala270Thr