Canonical Allele Identifier: CA388787175

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773282A>C (hg19) ; chr13:g.113118968A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118968A>C , CM000675.2:g.113118968A>C	GRCh38
NC_000013.10:g.113773282A>C , CM000675.1:g.113773282A>C	GRCh37
NC_000013.9:g.112821283A>C	NCBI36
NG_009258.1:g.1170A>C , LRG_548:g.1170A>C
NG_009262.1:g.18178A>C , LRG_554:g.18178A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1295A>C MANE Select	ENSP00000329546.4:p.Glu432Ala
ENST00000346342.7:c.1295A>C	ENSP00000329546.3:p.Glu432Ala
ENST00000375581.3:c.1361A>C	ENSP00000364731.3:p.Glu454Ala
ENST00000541084.5:c.1109A>C	ENSP00000442051.2:p.Glu370Ala
NM_000131.4:c.1361A>C , LRG_554t1:c.1361A>C	NP_000122.1:p.Glu454Ala
NM_001267554.1:c.1109A>C	NP_001254483.1:p.Glu370Ala
NM_019616.3:c.1295A>C , LRG_554t2:c.1295A>C	NP_062562.1:p.Glu432Ala
NR_051961.1:n.1382A>C
XM_006719963.2:c.1154A>C	XP_006720026.1:p.Glu385Ala
XM_011537474.1:c.1403A>C	XP_011535776.1:p.Glu468Ala
XM_011537475.1:c.1217A>C	XP_011535777.1:p.Glu406Ala
XM_011537476.1:c.1055A>C	XP_011535778.1:p.Glu352Ala
XM_011537477.1:c.1364A>C	XP_011535779.1:p.Glu455Ala
XM_006719963.3:c.1199A>C	XP_006720026.2:p.Glu400Ala
XM_011537474.2:c.1448A>C	XP_011535776.2:p.Glu483Ala
XM_011537475.2:c.1262A>C	XP_011535777.2:p.Glu421Ala
XM_011537476.2:c.1055A>C	XP_011535778.1:p.Glu352Ala
NM_019616.4:c.1295A>C MANE Select	NP_062562.1:p.Glu432Ala
NR_051961.2:n.1379A>C
NM_001267554.2:c.1109A>C	NP_001254483.1:p.Glu370Ala