Canonical Allele Identifier: CA388786006

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772850A>C (hg19) ; chr13:g.113118536A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118536A>C , CM000675.2:g.113118536A>C	GRCh38
NC_000013.10:g.113772850A>C , CM000675.1:g.113772850A>C	GRCh37
NC_000013.9:g.112820851A>C	NCBI36
NG_009258.1:g.738A>C , LRG_548:g.738A>C
NG_009262.1:g.17746A>C , LRG_554:g.17746A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.863A>C MANE Select	ENSP00000329546.4:p.Gln288Pro
ENST00000346342.7:c.863A>C	ENSP00000329546.3:p.Gln288Pro
ENST00000375581.3:c.929A>C	ENSP00000364731.3:p.Gln310Pro
ENST00000541084.5:c.677A>C	ENSP00000442051.2:p.Gln226Pro
NM_000131.4:c.929A>C , LRG_554t1:c.929A>C	NP_000122.1:p.Gln310Pro
NM_001267554.1:c.677A>C	NP_001254483.1:p.Gln226Pro
NM_019616.3:c.863A>C , LRG_554t2:c.863A>C	NP_062562.1:p.Gln288Pro
NR_051961.1:n.950A>C
XM_006719963.2:c.722A>C	XP_006720026.1:p.Gln241Pro
XM_011537474.1:c.971A>C	XP_011535776.1:p.Gln324Pro
XM_011537475.1:c.785A>C	XP_011535777.1:p.Gln262Pro
XM_011537476.1:c.623A>C	XP_011535778.1:p.Gln208Pro
XM_011537477.1:c.932A>C	XP_011535779.1:p.Gln311Pro
XM_006719963.3:c.767A>C	XP_006720026.2:p.Gln256Pro
XM_011537474.2:c.1016A>C	XP_011535776.2:p.Gln339Pro
XM_011537475.2:c.830A>C	XP_011535777.2:p.Gln277Pro
XM_011537476.2:c.623A>C	XP_011535778.1:p.Gln208Pro
NM_019616.4:c.863A>C MANE Select	NP_062562.1:p.Gln288Pro
NR_051961.2:n.947A>C
NM_001267554.2:c.677A>C	NP_001254483.1:p.Gln226Pro