Canonical Allele Identifier: CA388787161

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773274G>C (hg19) ; chr13:g.113118960G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118960G>C , CM000675.2:g.113118960G>C	GRCh38
NC_000013.10:g.113773274G>C , CM000675.1:g.113773274G>C	GRCh37
NC_000013.9:g.112821275G>C	NCBI36
NG_009258.1:g.1162G>C , LRG_548:g.1162G>C
NG_009262.1:g.18170G>C , LRG_554:g.18170G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1287G>C MANE Select	ENSP00000329546.4:p.Met429Ile
ENST00000346342.7:c.1287G>C	ENSP00000329546.3:p.Met429Ile
ENST00000375581.3:c.1353G>C	ENSP00000364731.3:p.Met451Ile
ENST00000541084.5:c.1101G>C	ENSP00000442051.2:p.Met367Ile
NM_000131.4:c.1353G>C , LRG_554t1:c.1353G>C	NP_000122.1:p.Met451Ile
NM_001267554.1:c.1101G>C	NP_001254483.1:p.Met367Ile
NM_019616.3:c.1287G>C , LRG_554t2:c.1287G>C	NP_062562.1:p.Met429Ile
NR_051961.1:n.1374G>C
XM_006719963.2:c.1146G>C	XP_006720026.1:p.Met382Ile
XM_011537474.1:c.1395G>C	XP_011535776.1:p.Met465Ile
XM_011537475.1:c.1209G>C	XP_011535777.1:p.Met403Ile
XM_011537476.1:c.1047G>C	XP_011535778.1:p.Met349Ile
XM_011537477.1:c.1356G>C	XP_011535779.1:p.Met452Ile
XM_006719963.3:c.1191G>C	XP_006720026.2:p.Met397Ile
XM_011537474.2:c.1440G>C	XP_011535776.2:p.Met480Ile
XM_011537475.2:c.1254G>C	XP_011535777.2:p.Met418Ile
XM_011537476.2:c.1047G>C	XP_011535778.1:p.Met349Ile
NM_019616.4:c.1287G>C MANE Select	NP_062562.1:p.Met429Ile
NR_051961.2:n.1371G>C
NM_001267554.2:c.1101G>C	NP_001254483.1:p.Met367Ile