Canonical Allele Identifier: CA388787157

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773273T>C (hg19) ; chr13:g.113118959T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118959T>C , CM000675.2:g.113118959T>C	GRCh38
NC_000013.10:g.113773273T>C , CM000675.1:g.113773273T>C	GRCh37
NC_000013.9:g.112821274T>C	NCBI36
NG_009258.1:g.1161T>C , LRG_548:g.1161T>C
NG_009262.1:g.18169T>C , LRG_554:g.18169T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1286T>C MANE Select	ENSP00000329546.4:p.Met429Thr
ENST00000346342.7:c.1286T>C	ENSP00000329546.3:p.Met429Thr
ENST00000375581.3:c.1352T>C	ENSP00000364731.3:p.Met451Thr
ENST00000541084.5:c.1100T>C	ENSP00000442051.2:p.Met367Thr
NM_000131.4:c.1352T>C , LRG_554t1:c.1352T>C	NP_000122.1:p.Met451Thr
NM_001267554.1:c.1100T>C	NP_001254483.1:p.Met367Thr
NM_019616.3:c.1286T>C , LRG_554t2:c.1286T>C	NP_062562.1:p.Met429Thr
NR_051961.1:n.1373T>C
XM_006719963.2:c.1145T>C	XP_006720026.1:p.Met382Thr
XM_011537474.1:c.1394T>C	XP_011535776.1:p.Met465Thr
XM_011537475.1:c.1208T>C	XP_011535777.1:p.Met403Thr
XM_011537476.1:c.1046T>C	XP_011535778.1:p.Met349Thr
XM_011537477.1:c.1355T>C	XP_011535779.1:p.Met452Thr
XM_006719963.3:c.1190T>C	XP_006720026.2:p.Met397Thr
XM_011537474.2:c.1439T>C	XP_011535776.2:p.Met480Thr
XM_011537475.2:c.1253T>C	XP_011535777.2:p.Met418Thr
XM_011537476.2:c.1046T>C	XP_011535778.1:p.Met349Thr
NM_019616.4:c.1286T>C MANE Select	NP_062562.1:p.Met429Thr
NR_051961.2:n.1370T>C
NM_001267554.2:c.1100T>C	NP_001254483.1:p.Met367Thr