Canonical Allele Identifier: CA485021760

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773310C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118996C>A , CM000675.2:g.113118996C>A	GRCh38
NC_000013.10:g.113773310C>A , CM000675.1:g.113773310C>A	GRCh37
NC_000013.9:g.112821311C>A	NCBI36
NG_009258.1:g.1198C>A , LRG_548:g.1198C>A
NG_009262.1:g.18206C>A , LRG_554:g.18206C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1323C>A MANE Select	ENSP00000329546.4:p.Ala441=
ENST00000346342.7:c.1323C>A	ENSP00000329546.3:p.Ala441=
ENST00000375581.3:c.1389C>A	ENSP00000364731.3:p.Ala463=
ENST00000541084.5:c.1137C>A	ENSP00000442051.2:p.Ala379=
NM_000131.4:c.1389C>A , LRG_554t1:c.1389C>A	NP_000122.1:p.Ala463=
NM_001267554.1:c.1137C>A	NP_001254483.1:p.Ala379=
NM_019616.3:c.1323C>A , LRG_554t2:c.1323C>A	NP_062562.1:p.Ala441=
NR_051961.1:n.1410C>A
XM_006719963.2:c.1182C>A	XP_006720026.1:p.Ala394=
XM_011537474.1:c.1431C>A	XP_011535776.1:p.Ala477=
XM_011537475.1:c.1245C>A	XP_011535777.1:p.Ala415=
XM_011537476.1:c.1083C>A	XP_011535778.1:p.Ala361=
XM_011537477.1:c.1392C>A	XP_011535779.1:p.Ala464=
XM_006719963.3:c.1227C>A	XP_006720026.2:p.Ala409=
XM_011537474.2:c.1476C>A	XP_011535776.2:p.Ala492=
XM_011537475.2:c.1290C>A	XP_011535777.2:p.Ala430=
XM_011537476.2:c.1083C>A	XP_011535778.1:p.Ala361=
NM_019616.4:c.1323C>A MANE Select	NP_062562.1:p.Ala441=
NR_051961.2:n.1407C>A
NM_001267554.2:c.1137C>A	NP_001254483.1:p.Ala379=