Canonical Allele Identifier: CA388785814

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772751A>C (hg19) ; chr13:g.113118437A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118437A>C , CM000675.2:g.113118437A>C	GRCh38
NC_000013.10:g.113772751A>C , CM000675.1:g.113772751A>C	GRCh37
NC_000013.9:g.112820752A>C	NCBI36
NG_009258.1:g.639A>C , LRG_548:g.639A>C
NG_009262.1:g.17647A>C , LRG_554:g.17647A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.764A>C MANE Select	ENSP00000329546.4:p.Asp255Ala
ENST00000346342.7:c.764A>C	ENSP00000329546.3:p.Asp255Ala
ENST00000375581.3:c.830A>C	ENSP00000364731.3:p.Asp277Ala
ENST00000541084.5:c.578A>C	ENSP00000442051.2:p.Asp193Ala
NM_000131.4:c.830A>C , LRG_554t1:c.830A>C	NP_000122.1:p.Asp277Ala
NM_001267554.1:c.578A>C	NP_001254483.1:p.Asp193Ala
NM_019616.3:c.764A>C , LRG_554t2:c.764A>C	NP_062562.1:p.Asp255Ala
NR_051961.1:n.851A>C
XM_006719963.2:c.623A>C	XP_006720026.1:p.Asp208Ala
XM_011537474.1:c.872A>C	XP_011535776.1:p.Asp291Ala
XM_011537475.1:c.686A>C	XP_011535777.1:p.Asp229Ala
XM_011537476.1:c.524A>C	XP_011535778.1:p.Asp175Ala
XM_011537477.1:c.833A>C	XP_011535779.1:p.Asp278Ala
XM_006719963.3:c.668A>C	XP_006720026.2:p.Asp223Ala
XM_011537474.2:c.917A>C	XP_011535776.2:p.Asp306Ala
XM_011537475.2:c.731A>C	XP_011535777.2:p.Asp244Ala
XM_011537476.2:c.524A>C	XP_011535778.1:p.Asp175Ala
NM_019616.4:c.764A>C MANE Select	NP_062562.1:p.Asp255Ala
NR_051961.2:n.848A>C
NM_001267554.2:c.578A>C	NP_001254483.1:p.Asp193Ala