Canonical Allele Identifier: CA485424034

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773064A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118750A>T , CM000675.2:g.113118750A>T	GRCh38
NC_000013.10:g.113773064A>T , CM000675.1:g.113773064A>T	GRCh37
NC_000013.9:g.112821065A>T	NCBI36
NG_009258.1:g.952A>T , LRG_548:g.952A>T
NG_009262.1:g.17960A>T , LRG_554:g.17960A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1077A>T MANE Select	ENSP00000329546.4:p.Pro359=
ENST00000346342.7:c.1077A>T	ENSP00000329546.3:p.Pro359=
ENST00000375581.3:c.1143A>T	ENSP00000364731.3:p.Pro381=
ENST00000541084.5:c.891A>T	ENSP00000442051.2:p.Pro297=
NM_000131.4:c.1143A>T , LRG_554t1:c.1143A>T	NP_000122.1:p.Pro381=
NM_001267554.1:c.891A>T	NP_001254483.1:p.Pro297=
NM_019616.3:c.1077A>T , LRG_554t2:c.1077A>T	NP_062562.1:p.Pro359=
NR_051961.1:n.1164A>T
XM_006719963.2:c.936A>T	XP_006720026.1:p.Pro312=
XM_011537474.1:c.1185A>T	XP_011535776.1:p.Pro395=
XM_011537475.1:c.999A>T	XP_011535777.1:p.Pro333=
XM_011537476.1:c.837A>T	XP_011535778.1:p.Pro279=
XM_011537477.1:c.1146A>T	XP_011535779.1:p.Pro382=
XM_006719963.3:c.981A>T	XP_006720026.2:p.Pro327=
XM_011537474.2:c.1230A>T	XP_011535776.2:p.Pro410=
XM_011537475.2:c.1044A>T	XP_011535777.2:p.Pro348=
XM_011537476.2:c.837A>T	XP_011535778.1:p.Pro279=
NM_019616.4:c.1077A>T MANE Select	NP_062562.1:p.Pro359=
NR_051961.2:n.1161A>T
NM_001267554.2:c.891A>T	NP_001254483.1:p.Pro297=