Canonical Allele Identifier: CA485021203

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773142A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118828A>G , CM000675.2:g.113118828A>G	GRCh38
NC_000013.10:g.113773142A>G , CM000675.1:g.113773142A>G	GRCh37
NC_000013.9:g.112821143A>G	NCBI36
NG_009258.1:g.1030A>G , LRG_548:g.1030A>G
NG_009262.1:g.18038A>G , LRG_554:g.18038A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1155A>G MANE Select	ENSP00000329546.4:p.Pro385=
ENST00000346342.7:c.1155A>G	ENSP00000329546.3:p.Pro385=
ENST00000375581.3:c.1221A>G	ENSP00000364731.3:p.Pro407=
ENST00000541084.5:c.969A>G	ENSP00000442051.2:p.Pro323=
NM_000131.4:c.1221A>G , LRG_554t1:c.1221A>G	NP_000122.1:p.Pro407=
NM_001267554.1:c.969A>G	NP_001254483.1:p.Pro323=
NM_019616.3:c.1155A>G , LRG_554t2:c.1155A>G	NP_062562.1:p.Pro385=
NR_051961.1:n.1242A>G
XM_006719963.2:c.1014A>G	XP_006720026.1:p.Pro338=
XM_011537474.1:c.1263A>G	XP_011535776.1:p.Pro421=
XM_011537475.1:c.1077A>G	XP_011535777.1:p.Pro359=
XM_011537476.1:c.915A>G	XP_011535778.1:p.Pro305=
XM_011537477.1:c.1224A>G	XP_011535779.1:p.Pro408=
XM_006719963.3:c.1059A>G	XP_006720026.2:p.Pro353=
XM_011537474.2:c.1308A>G	XP_011535776.2:p.Pro436=
XM_011537475.2:c.1122A>G	XP_011535777.2:p.Pro374=
XM_011537476.2:c.915A>G	XP_011535778.1:p.Pro305=
NM_019616.4:c.1155A>G MANE Select	NP_062562.1:p.Pro385=
NR_051961.2:n.1239A>G
NM_001267554.2:c.969A>G	NP_001254483.1:p.Pro323=