Canonical Allele Identifier: CA388786661

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773114A>C (hg19) ; chr13:g.113118800A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118800A>C , CM000675.2:g.113118800A>C	GRCh38
NC_000013.10:g.113773114A>C , CM000675.1:g.113773114A>C	GRCh37
NC_000013.9:g.112821115A>C	NCBI36
NG_009258.1:g.1002A>C , LRG_548:g.1002A>C
NG_009262.1:g.18010A>C , LRG_554:g.18010A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1127A>C MANE Select	ENSP00000329546.4:p.Asp376Ala
ENST00000346342.7:c.1127A>C	ENSP00000329546.3:p.Asp376Ala
ENST00000375581.3:c.1193A>C	ENSP00000364731.3:p.Asp398Ala
ENST00000541084.5:c.941A>C	ENSP00000442051.2:p.Asp314Ala
NM_000131.4:c.1193A>C , LRG_554t1:c.1193A>C	NP_000122.1:p.Asp398Ala
NM_001267554.1:c.941A>C	NP_001254483.1:p.Asp314Ala
NM_019616.3:c.1127A>C , LRG_554t2:c.1127A>C	NP_062562.1:p.Asp376Ala
NR_051961.1:n.1214A>C
XM_006719963.2:c.986A>C	XP_006720026.1:p.Asp329Ala
XM_011537474.1:c.1235A>C	XP_011535776.1:p.Asp412Ala
XM_011537475.1:c.1049A>C	XP_011535777.1:p.Asp350Ala
XM_011537476.1:c.887A>C	XP_011535778.1:p.Asp296Ala
XM_011537477.1:c.1196A>C	XP_011535779.1:p.Asp399Ala
XM_006719963.3:c.1031A>C	XP_006720026.2:p.Asp344Ala
XM_011537474.2:c.1280A>C	XP_011535776.2:p.Asp427Ala
XM_011537475.2:c.1094A>C	XP_011535777.2:p.Asp365Ala
XM_011537476.2:c.887A>C	XP_011535778.1:p.Asp296Ala
NM_019616.4:c.1127A>C MANE Select	NP_062562.1:p.Asp376Ala
NR_051961.2:n.1211A>C
NM_001267554.2:c.941A>C	NP_001254483.1:p.Asp314Ala