Canonical Allele Identifier: CA388785866

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772778C>G (hg19) ; chr13:g.113118464C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118464C>G , CM000675.2:g.113118464C>G	GRCh38
NC_000013.10:g.113772778C>G , CM000675.1:g.113772778C>G	GRCh37
NC_000013.9:g.112820779C>G	NCBI36
NG_009258.1:g.666C>G , LRG_548:g.666C>G
NG_009262.1:g.17674C>G , LRG_554:g.17674C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.791C>G MANE Select	ENSP00000329546.4:p.Ala264Gly
ENST00000346342.7:c.791C>G	ENSP00000329546.3:p.Ala264Gly
ENST00000375581.3:c.857C>G	ENSP00000364731.3:p.Ala286Gly
ENST00000541084.5:c.605C>G	ENSP00000442051.2:p.Ala202Gly
NM_000131.4:c.857C>G , LRG_554t1:c.857C>G	NP_000122.1:p.Ala286Gly
NM_001267554.1:c.605C>G	NP_001254483.1:p.Ala202Gly
NM_019616.3:c.791C>G , LRG_554t2:c.791C>G	NP_062562.1:p.Ala264Gly
NR_051961.1:n.878C>G
XM_006719963.2:c.650C>G	XP_006720026.1:p.Ala217Gly
XM_011537474.1:c.899C>G	XP_011535776.1:p.Ala300Gly
XM_011537475.1:c.713C>G	XP_011535777.1:p.Ala238Gly
XM_011537476.1:c.551C>G	XP_011535778.1:p.Ala184Gly
XM_011537477.1:c.860C>G	XP_011535779.1:p.Ala287Gly
XM_006719963.3:c.695C>G	XP_006720026.2:p.Ala232Gly
XM_011537474.2:c.944C>G	XP_011535776.2:p.Ala315Gly
XM_011537475.2:c.758C>G	XP_011535777.2:p.Ala253Gly
XM_011537476.2:c.551C>G	XP_011535778.1:p.Ala184Gly
NM_019616.4:c.791C>G MANE Select	NP_062562.1:p.Ala264Gly
NR_051961.2:n.875C>G
NM_001267554.2:c.605C>G	NP_001254483.1:p.Ala202Gly