Canonical Allele Identifier: CA7060159

Gene: F7

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118495G>A , CM000675.2:g.113118495G>A	GRCh38
NC_000013.10:g.113772809G>A , CM000675.1:g.113772809G>A	GRCh37
NC_000013.9:g.112820810G>A	NCBI36
NG_009258.1:g.697G>A , LRG_548:g.697G>A
NG_009262.1:g.17705G>A , LRG_554:g.17705G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_019616.4:c.822G>A MANE Select	NP_062562.1:p.Pro274=
ENST00000346342.8:c.822G>A MANE Select	ENSP00000329546.4:p.Pro274=
NM_000131.4:c.888G>A , LRG_554t1:c.888G>A	NP_000122.1:p.Pro296=
NM_001267554.1:c.636G>A	NP_001254483.1:p.Pro212=
NM_001267554.2:c.636G>A	NP_001254483.1:p.Pro212=
NM_019616.3:c.822G>A , LRG_554t2:c.822G>A	NP_062562.1:p.Pro274=
NR_051961.1:n.909G>A
NR_051961.2:n.906G>A
ENST00000346342.7:c.822G>A	ENSP00000329546.3:p.Pro274=
ENST00000375581.3:c.888G>A	ENSP00000364731.3:p.Pro296=
ENST00000541084.5:c.636G>A	ENSP00000442051.2:p.Pro212=
XM_006719963.2:c.681G>A	XP_006720026.1:p.Pro227=
XM_006719963.3:c.726G>A	XP_006720026.2:p.Pro242=
XM_011537474.1:c.930G>A	XP_011535776.1:p.Pro310=
XM_011537474.2:c.975G>A	XP_011535776.2:p.Pro325=
XM_011537475.1:c.744G>A	XP_011535777.1:p.Pro248=
XM_011537475.2:c.789G>A	XP_011535777.2:p.Pro263=
XM_011537476.1:c.582G>A	XP_011535778.1:p.Pro194=
XM_011537476.2:c.582G>A	XP_011535778.1:p.Pro194=
XM_011537477.1:c.891G>A	XP_011535779.1:p.Pro297=