Canonical Allele Identifier: CA388785924

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772807C>G (hg19) ; chr13:g.113118493C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118493C>G , CM000675.2:g.113118493C>G	GRCh38
NC_000013.10:g.113772807C>G , CM000675.1:g.113772807C>G	GRCh37
NC_000013.9:g.112820808C>G	NCBI36
NG_009258.1:g.695C>G , LRG_548:g.695C>G
NG_009262.1:g.17703C>G , LRG_554:g.17703C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.820C>G MANE Select	ENSP00000329546.4:p.Pro274Ala
ENST00000346342.7:c.820C>G	ENSP00000329546.3:p.Pro274Ala
ENST00000375581.3:c.886C>G	ENSP00000364731.3:p.Pro296Ala
ENST00000541084.5:c.634C>G	ENSP00000442051.2:p.Pro212Ala
NM_000131.4:c.886C>G , LRG_554t1:c.886C>G	NP_000122.1:p.Pro296Ala
NM_001267554.1:c.634C>G	NP_001254483.1:p.Pro212Ala
NM_019616.3:c.820C>G , LRG_554t2:c.820C>G	NP_062562.1:p.Pro274Ala
NR_051961.1:n.907C>G
XM_006719963.2:c.679C>G	XP_006720026.1:p.Pro227Ala
XM_011537474.1:c.928C>G	XP_011535776.1:p.Pro310Ala
XM_011537475.1:c.742C>G	XP_011535777.1:p.Pro248Ala
XM_011537476.1:c.580C>G	XP_011535778.1:p.Pro194Ala
XM_011537477.1:c.889C>G	XP_011535779.1:p.Pro297Ala
XM_006719963.3:c.724C>G	XP_006720026.2:p.Pro242Ala
XM_011537474.2:c.973C>G	XP_011535776.2:p.Pro325Ala
XM_011537475.2:c.787C>G	XP_011535777.2:p.Pro263Ala
XM_011537476.2:c.580C>G	XP_011535778.1:p.Pro194Ala
NM_019616.4:c.820C>G MANE Select	NP_062562.1:p.Pro274Ala
NR_051961.2:n.904C>G
NM_001267554.2:c.634C>G	NP_001254483.1:p.Pro212Ala