Canonical Allele Identifier: CA388787187

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773288G>C (hg19) ; chr13:g.113118974G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118974G>C , CM000675.2:g.113118974G>C	GRCh38
NC_000013.10:g.113773288G>C , CM000675.1:g.113773288G>C	GRCh37
NC_000013.9:g.112821289G>C	NCBI36
NG_009258.1:g.1176G>C , LRG_548:g.1176G>C
NG_009262.1:g.18184G>C , LRG_554:g.18184G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1301G>C MANE Select	ENSP00000329546.4:p.Arg434Pro
ENST00000346342.7:c.1301G>C	ENSP00000329546.3:p.Arg434Pro
ENST00000375581.3:c.1367G>C	ENSP00000364731.3:p.Arg456Pro
ENST00000541084.5:c.1115G>C	ENSP00000442051.2:p.Arg372Pro
NM_000131.4:c.1367G>C , LRG_554t1:c.1367G>C	NP_000122.1:p.Arg456Pro
NM_001267554.1:c.1115G>C	NP_001254483.1:p.Arg372Pro
NM_019616.3:c.1301G>C , LRG_554t2:c.1301G>C	NP_062562.1:p.Arg434Pro
NR_051961.1:n.1388G>C
XM_006719963.2:c.1160G>C	XP_006720026.1:p.Arg387Pro
XM_011537474.1:c.1409G>C	XP_011535776.1:p.Arg470Pro
XM_011537475.1:c.1223G>C	XP_011535777.1:p.Arg408Pro
XM_011537476.1:c.1061G>C	XP_011535778.1:p.Arg354Pro
XM_011537477.1:c.1370G>C	XP_011535779.1:p.Arg457Pro
XM_006719963.3:c.1205G>C	XP_006720026.2:p.Arg402Pro
XM_011537474.2:c.1454G>C	XP_011535776.2:p.Arg485Pro
XM_011537475.2:c.1268G>C	XP_011535777.2:p.Arg423Pro
XM_011537476.2:c.1061G>C	XP_011535778.1:p.Arg354Pro
NM_019616.4:c.1301G>C MANE Select	NP_062562.1:p.Arg434Pro
NR_051961.2:n.1385G>C
NM_001267554.2:c.1115G>C	NP_001254483.1:p.Arg372Pro