Canonical Allele Identifier: CA388786331

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773018T>A (hg19) ; chr13:g.113118704T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118704T>A , CM000675.2:g.113118704T>A	GRCh38
NC_000013.10:g.113773018T>A , CM000675.1:g.113773018T>A	GRCh37
NC_000013.9:g.112821019T>A	NCBI36
NG_009258.1:g.906T>A , LRG_548:g.906T>A
NG_009262.1:g.17914T>A , LRG_554:g.17914T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1031T>A MANE Select	ENSP00000329546.4:p.Met344Lys
ENST00000346342.7:c.1031T>A	ENSP00000329546.3:p.Met344Lys
ENST00000375581.3:c.1097T>A	ENSP00000364731.3:p.Met366Lys
ENST00000541084.5:c.845T>A	ENSP00000442051.2:p.Met282Lys
NM_000131.4:c.1097T>A , LRG_554t1:c.1097T>A	NP_000122.1:p.Met366Lys
NM_001267554.1:c.845T>A	NP_001254483.1:p.Met282Lys
NM_019616.3:c.1031T>A , LRG_554t2:c.1031T>A	NP_062562.1:p.Met344Lys
NR_051961.1:n.1118T>A
XM_006719963.2:c.890T>A	XP_006720026.1:p.Met297Lys
XM_011537474.1:c.1139T>A	XP_011535776.1:p.Met380Lys
XM_011537475.1:c.953T>A	XP_011535777.1:p.Met318Lys
XM_011537476.1:c.791T>A	XP_011535778.1:p.Met264Lys
XM_011537477.1:c.1100T>A	XP_011535779.1:p.Met367Lys
XM_006719963.3:c.935T>A	XP_006720026.2:p.Met312Lys
XM_011537474.2:c.1184T>A	XP_011535776.2:p.Met395Lys
XM_011537475.2:c.998T>A	XP_011535777.2:p.Met333Lys
XM_011537476.2:c.791T>A	XP_011535778.1:p.Met264Lys
NM_019616.4:c.1031T>A MANE Select	NP_062562.1:p.Met344Lys
NR_051961.2:n.1115T>A
NM_001267554.2:c.845T>A	NP_001254483.1:p.Met282Lys