Canonical Allele Identifier: CA388785910

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772798A>T (hg19) ; chr13:g.113118484A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118484A>T , CM000675.2:g.113118484A>T	GRCh38
NC_000013.10:g.113772798A>T , CM000675.1:g.113772798A>T	GRCh37
NC_000013.9:g.112820799A>T	NCBI36
NG_009258.1:g.686A>T , LRG_548:g.686A>T
NG_009262.1:g.17694A>T , LRG_554:g.17694A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.811A>T MANE Select	ENSP00000329546.4:p.Thr271Ser
ENST00000346342.7:c.811A>T	ENSP00000329546.3:p.Thr271Ser
ENST00000375581.3:c.877A>T	ENSP00000364731.3:p.Thr293Ser
ENST00000541084.5:c.625A>T	ENSP00000442051.2:p.Thr209Ser
NM_000131.4:c.877A>T , LRG_554t1:c.877A>T	NP_000122.1:p.Thr293Ser
NM_001267554.1:c.625A>T	NP_001254483.1:p.Thr209Ser
NM_019616.3:c.811A>T , LRG_554t2:c.811A>T	NP_062562.1:p.Thr271Ser
NR_051961.1:n.898A>T
XM_006719963.2:c.670A>T	XP_006720026.1:p.Thr224Ser
XM_011537474.1:c.919A>T	XP_011535776.1:p.Thr307Ser
XM_011537475.1:c.733A>T	XP_011535777.1:p.Thr245Ser
XM_011537476.1:c.571A>T	XP_011535778.1:p.Thr191Ser
XM_011537477.1:c.880A>T	XP_011535779.1:p.Thr294Ser
XM_006719963.3:c.715A>T	XP_006720026.2:p.Thr239Ser
XM_011537474.2:c.964A>T	XP_011535776.2:p.Thr322Ser
XM_011537475.2:c.778A>T	XP_011535777.2:p.Thr260Ser
XM_011537476.2:c.571A>T	XP_011535778.1:p.Thr191Ser
NM_019616.4:c.811A>T MANE Select	NP_062562.1:p.Thr271Ser
NR_051961.2:n.895A>T
NM_001267554.2:c.625A>T	NP_001254483.1:p.Thr209Ser