Canonical Allele Identifier: CA388786217

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772955G>C (hg19) ; chr13:g.113118641G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118641G>C , CM000675.2:g.113118641G>C	GRCh38
NC_000013.10:g.113772955G>C , CM000675.1:g.113772955G>C	GRCh37
NC_000013.9:g.112820956G>C	NCBI36
NG_009258.1:g.843G>C , LRG_548:g.843G>C
NG_009262.1:g.17851G>C , LRG_554:g.17851G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.968G>C MANE Select	ENSP00000329546.4:p.Gly323Ala
ENST00000346342.7:c.968G>C	ENSP00000329546.3:p.Gly323Ala
ENST00000375581.3:c.1034G>C	ENSP00000364731.3:p.Gly345Ala
ENST00000541084.5:c.782G>C	ENSP00000442051.2:p.Gly261Ala
NM_000131.4:c.1034G>C , LRG_554t1:c.1034G>C	NP_000122.1:p.Gly345Ala
NM_001267554.1:c.782G>C	NP_001254483.1:p.Gly261Ala
NM_019616.3:c.968G>C , LRG_554t2:c.968G>C	NP_062562.1:p.Gly323Ala
NR_051961.1:n.1055G>C
XM_006719963.2:c.827G>C	XP_006720026.1:p.Gly276Ala
XM_011537474.1:c.1076G>C	XP_011535776.1:p.Gly359Ala
XM_011537475.1:c.890G>C	XP_011535777.1:p.Gly297Ala
XM_011537476.1:c.728G>C	XP_011535778.1:p.Gly243Ala
XM_011537477.1:c.1037G>C	XP_011535779.1:p.Gly346Ala
XM_006719963.3:c.872G>C	XP_006720026.2:p.Gly291Ala
XM_011537474.2:c.1121G>C	XP_011535776.2:p.Gly374Ala
XM_011537475.2:c.935G>C	XP_011535777.2:p.Gly312Ala
XM_011537476.2:c.728G>C	XP_011535778.1:p.Gly243Ala
NM_019616.4:c.968G>C MANE Select	NP_062562.1:p.Gly323Ala
NR_051961.2:n.1052G>C
NM_001267554.2:c.782G>C	NP_001254483.1:p.Gly261Ala