Canonical Allele Identifier: CA485021620

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773286A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118972A>C , CM000675.2:g.113118972A>C	GRCh38
NC_000013.10:g.113773286A>C , CM000675.1:g.113773286A>C	GRCh37
NC_000013.9:g.112821287A>C	NCBI36
NG_009258.1:g.1174A>C , LRG_548:g.1174A>C
NG_009262.1:g.18182A>C , LRG_554:g.18182A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1299A>C MANE Select	ENSP00000329546.4:p.Pro433=
ENST00000346342.7:c.1299A>C	ENSP00000329546.3:p.Pro433=
ENST00000375581.3:c.1365A>C	ENSP00000364731.3:p.Pro455=
ENST00000541084.5:c.1113A>C	ENSP00000442051.2:p.Pro371=
NM_000131.4:c.1365A>C , LRG_554t1:c.1365A>C	NP_000122.1:p.Pro455=
NM_001267554.1:c.1113A>C	NP_001254483.1:p.Pro371=
NM_019616.3:c.1299A>C , LRG_554t2:c.1299A>C	NP_062562.1:p.Pro433=
NR_051961.1:n.1386A>C
XM_006719963.2:c.1158A>C	XP_006720026.1:p.Pro386=
XM_011537474.1:c.1407A>C	XP_011535776.1:p.Pro469=
XM_011537475.1:c.1221A>C	XP_011535777.1:p.Pro407=
XM_011537476.1:c.1059A>C	XP_011535778.1:p.Pro353=
XM_011537477.1:c.1368A>C	XP_011535779.1:p.Pro456=
XM_006719963.3:c.1203A>C	XP_006720026.2:p.Pro401=
XM_011537474.2:c.1452A>C	XP_011535776.2:p.Pro484=
XM_011537475.2:c.1266A>C	XP_011535777.2:p.Pro422=
XM_011537476.2:c.1059A>C	XP_011535778.1:p.Pro353=
NM_019616.4:c.1299A>C MANE Select	NP_062562.1:p.Pro433=
NR_051961.2:n.1383A>C
NM_001267554.2:c.1113A>C	NP_001254483.1:p.Pro371=