Canonical Allele Identifier: CA388787167

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773278T>C (hg19) ; chr13:g.113118964T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118964T>C , CM000675.2:g.113118964T>C	GRCh38
NC_000013.10:g.113773278T>C , CM000675.1:g.113773278T>C	GRCh37
NC_000013.9:g.112821279T>C	NCBI36
NG_009258.1:g.1166T>C , LRG_548:g.1166T>C
NG_009262.1:g.18174T>C , LRG_554:g.18174T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1291T>C MANE Select	ENSP00000329546.4:p.Ser431Pro
ENST00000346342.7:c.1291T>C	ENSP00000329546.3:p.Ser431Pro
ENST00000375581.3:c.1357T>C	ENSP00000364731.3:p.Ser453Pro
ENST00000541084.5:c.1105T>C	ENSP00000442051.2:p.Ser369Pro
NM_000131.4:c.1357T>C , LRG_554t1:c.1357T>C	NP_000122.1:p.Ser453Pro
NM_001267554.1:c.1105T>C	NP_001254483.1:p.Ser369Pro
NM_019616.3:c.1291T>C , LRG_554t2:c.1291T>C	NP_062562.1:p.Ser431Pro
NR_051961.1:n.1378T>C
XM_006719963.2:c.1150T>C	XP_006720026.1:p.Ser384Pro
XM_011537474.1:c.1399T>C	XP_011535776.1:p.Ser467Pro
XM_011537475.1:c.1213T>C	XP_011535777.1:p.Ser405Pro
XM_011537476.1:c.1051T>C	XP_011535778.1:p.Ser351Pro
XM_011537477.1:c.1360T>C	XP_011535779.1:p.Ser454Pro
XM_006719963.3:c.1195T>C	XP_006720026.2:p.Ser399Pro
XM_011537474.2:c.1444T>C	XP_011535776.2:p.Ser482Pro
XM_011537475.2:c.1258T>C	XP_011535777.2:p.Ser420Pro
XM_011537476.2:c.1051T>C	XP_011535778.1:p.Ser351Pro
NM_019616.4:c.1291T>C MANE Select	NP_062562.1:p.Ser431Pro
NR_051961.2:n.1375T>C
NM_001267554.2:c.1105T>C	NP_001254483.1:p.Ser369Pro