Canonical Allele Identifier: CA485021672

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773295A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118981A>C , CM000675.2:g.113118981A>C	GRCh38
NC_000013.10:g.113773295A>C , CM000675.1:g.113773295A>C	GRCh37
NC_000013.9:g.112821296A>C	NCBI36
NG_009258.1:g.1183A>C , LRG_548:g.1183A>C
NG_009262.1:g.18191A>C , LRG_554:g.18191A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1308A>C MANE Select	ENSP00000329546.4:p.Gly436=
ENST00000346342.7:c.1308A>C	ENSP00000329546.3:p.Gly436=
ENST00000375581.3:c.1374A>C	ENSP00000364731.3:p.Gly458=
ENST00000541084.5:c.1122A>C	ENSP00000442051.2:p.Gly374=
NM_000131.4:c.1374A>C , LRG_554t1:c.1374A>C	NP_000122.1:p.Gly458=
NM_001267554.1:c.1122A>C	NP_001254483.1:p.Gly374=
NM_019616.3:c.1308A>C , LRG_554t2:c.1308A>C	NP_062562.1:p.Gly436=
NR_051961.1:n.1395A>C
XM_006719963.2:c.1167A>C	XP_006720026.1:p.Gly389=
XM_011537474.1:c.1416A>C	XP_011535776.1:p.Gly472=
XM_011537475.1:c.1230A>C	XP_011535777.1:p.Gly410=
XM_011537476.1:c.1068A>C	XP_011535778.1:p.Gly356=
XM_011537477.1:c.1377A>C	XP_011535779.1:p.Gly459=
XM_006719963.3:c.1212A>C	XP_006720026.2:p.Gly404=
XM_011537474.2:c.1461A>C	XP_011535776.2:p.Gly487=
XM_011537475.2:c.1275A>C	XP_011535777.2:p.Gly425=
XM_011537476.2:c.1068A>C	XP_011535778.1:p.Gly356=
NM_019616.4:c.1308A>C MANE Select	NP_062562.1:p.Gly436=
NR_051961.2:n.1392A>C
NM_001267554.2:c.1122A>C	NP_001254483.1:p.Gly374=