Canonical Allele Identifier: CA388786133

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772915A>C (hg19) ; chr13:g.113118601A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118601A>C , CM000675.2:g.113118601A>C	GRCh38
NC_000013.10:g.113772915A>C , CM000675.1:g.113772915A>C	GRCh37
NC_000013.9:g.112820916A>C	NCBI36
NG_009258.1:g.803A>C , LRG_548:g.803A>C
NG_009262.1:g.17811A>C , LRG_554:g.17811A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.928A>C MANE Select	ENSP00000329546.4:p.Thr310Pro
ENST00000346342.7:c.928A>C	ENSP00000329546.3:p.Thr310Pro
ENST00000375581.3:c.994A>C	ENSP00000364731.3:p.Thr332Pro
ENST00000541084.5:c.742A>C	ENSP00000442051.2:p.Thr248Pro
NM_000131.4:c.994A>C , LRG_554t1:c.994A>C	NP_000122.1:p.Thr332Pro
NM_001267554.1:c.742A>C	NP_001254483.1:p.Thr248Pro
NM_019616.3:c.928A>C , LRG_554t2:c.928A>C	NP_062562.1:p.Thr310Pro
NR_051961.1:n.1015A>C
XM_006719963.2:c.787A>C	XP_006720026.1:p.Thr263Pro
XM_011537474.1:c.1036A>C	XP_011535776.1:p.Thr346Pro
XM_011537475.1:c.850A>C	XP_011535777.1:p.Thr284Pro
XM_011537476.1:c.688A>C	XP_011535778.1:p.Thr230Pro
XM_011537477.1:c.997A>C	XP_011535779.1:p.Thr333Pro
XM_006719963.3:c.832A>C	XP_006720026.2:p.Thr278Pro
XM_011537474.2:c.1081A>C	XP_011535776.2:p.Thr361Pro
XM_011537475.2:c.895A>C	XP_011535777.2:p.Thr299Pro
XM_011537476.2:c.688A>C	XP_011535778.1:p.Thr230Pro
NM_019616.4:c.928A>C MANE Select	NP_062562.1:p.Thr310Pro
NR_051961.2:n.1012A>C
NM_001267554.2:c.742A>C	NP_001254483.1:p.Thr248Pro