Canonical Allele Identifier: CA388785846

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772765A>C (hg19) ; chr13:g.113118451A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118451A>C , CM000675.2:g.113118451A>C	GRCh38
NC_000013.10:g.113772765A>C , CM000675.1:g.113772765A>C	GRCh37
NC_000013.9:g.112820766A>C	NCBI36
NG_009258.1:g.653A>C , LRG_548:g.653A>C
NG_009262.1:g.17661A>C , LRG_554:g.17661A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.778A>C MANE Select	ENSP00000329546.4:p.Ser260Arg
ENST00000346342.7:c.778A>C	ENSP00000329546.3:p.Ser260Arg
ENST00000375581.3:c.844A>C	ENSP00000364731.3:p.Ser282Arg
ENST00000541084.5:c.592A>C	ENSP00000442051.2:p.Ser198Arg
NM_000131.4:c.844A>C , LRG_554t1:c.844A>C	NP_000122.1:p.Ser282Arg
NM_001267554.1:c.592A>C	NP_001254483.1:p.Ser198Arg
NM_019616.3:c.778A>C , LRG_554t2:c.778A>C	NP_062562.1:p.Ser260Arg
NR_051961.1:n.865A>C
XM_006719963.2:c.637A>C	XP_006720026.1:p.Ser213Arg
XM_011537474.1:c.886A>C	XP_011535776.1:p.Ser296Arg
XM_011537475.1:c.700A>C	XP_011535777.1:p.Ser234Arg
XM_011537476.1:c.538A>C	XP_011535778.1:p.Ser180Arg
XM_011537477.1:c.847A>C	XP_011535779.1:p.Ser283Arg
XM_006719963.3:c.682A>C	XP_006720026.2:p.Ser228Arg
XM_011537474.2:c.931A>C	XP_011535776.2:p.Ser311Arg
XM_011537475.2:c.745A>C	XP_011535777.2:p.Ser249Arg
XM_011537476.2:c.538A>C	XP_011535778.1:p.Ser180Arg
NM_019616.4:c.778A>C MANE Select	NP_062562.1:p.Ser260Arg
NR_051961.2:n.862A>C
NM_001267554.2:c.592A>C	NP_001254483.1:p.Ser198Arg