Canonical Allele Identifier: CA7060150

Gene: F7

Linked Data

• dbSNP Id: rs368187411
• ExAC: 13:113772779 G / A
• gnomAD v2: 13-113772779-G-A
• gnomAD v3: 13-113118465-G-A
• gnomAD v4: 13-113118465-G-A
• COSMIC: COSM945536
• MyVariant Identifiers: chr13:g.113772779G>A (hg19) ; chr13:g.113118465G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118465G>A , CM000675.2:g.113118465G>A	GRCh38
NC_000013.10:g.113772779G>A , CM000675.1:g.113772779G>A	GRCh37
NC_000013.9:g.112820780G>A	NCBI36
NG_009258.1:g.667G>A , LRG_548:g.667G>A
NG_009262.1:g.17675G>A , LRG_554:g.17675G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.792G>A MANE Select	ENSP00000329546.4:p.Ala264=
ENST00000346342.7:c.792G>A	ENSP00000329546.3:p.Ala264=
ENST00000375581.3:c.858G>A	ENSP00000364731.3:p.Ala286=
ENST00000541084.5:c.606G>A	ENSP00000442051.2:p.Ala202=
NM_000131.4:c.858G>A , LRG_554t1:c.858G>A	NP_000122.1:p.Ala286=
NM_001267554.1:c.606G>A	NP_001254483.1:p.Ala202=
NM_019616.3:c.792G>A , LRG_554t2:c.792G>A	NP_062562.1:p.Ala264=
NR_051961.1:n.879G>A
XM_006719963.2:c.651G>A	XP_006720026.1:p.Ala217=
XM_011537474.1:c.900G>A	XP_011535776.1:p.Ala300=
XM_011537475.1:c.714G>A	XP_011535777.1:p.Ala238=
XM_011537476.1:c.552G>A	XP_011535778.1:p.Ala184=
XM_011537477.1:c.861G>A	XP_011535779.1:p.Ala287=
XM_006719963.3:c.696G>A	XP_006720026.2:p.Ala232=
XM_011537474.2:c.945G>A	XP_011535776.2:p.Ala315=
XM_011537475.2:c.759G>A	XP_011535777.2:p.Ala253=
XM_011537476.2:c.552G>A	XP_011535778.1:p.Ala184=
NM_019616.4:c.792G>A MANE Select	NP_062562.1:p.Ala264=
NR_051961.2:n.876G>A
NM_001267554.2:c.606G>A	NP_001254483.1:p.Ala202=