Canonical Allele Identifier: CA388785973

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772831G>C (hg19) ; chr13:g.113118517G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118517G>C , CM000675.2:g.113118517G>C	GRCh38
NC_000013.10:g.113772831G>C , CM000675.1:g.113772831G>C	GRCh37
NC_000013.9:g.112820832G>C	NCBI36
NG_009258.1:g.719G>C , LRG_548:g.719G>C
NG_009262.1:g.17727G>C , LRG_554:g.17727G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.844G>C MANE Select	ENSP00000329546.4:p.Ala282Pro
ENST00000346342.7:c.844G>C	ENSP00000329546.3:p.Ala282Pro
ENST00000375581.3:c.910G>C	ENSP00000364731.3:p.Ala304Pro
ENST00000541084.5:c.658G>C	ENSP00000442051.2:p.Ala220Pro
NM_000131.4:c.910G>C , LRG_554t1:c.910G>C	NP_000122.1:p.Ala304Pro
NM_001267554.1:c.658G>C	NP_001254483.1:p.Ala220Pro
NM_019616.3:c.844G>C , LRG_554t2:c.844G>C	NP_062562.1:p.Ala282Pro
NR_051961.1:n.931G>C
XM_006719963.2:c.703G>C	XP_006720026.1:p.Ala235Pro
XM_011537474.1:c.952G>C	XP_011535776.1:p.Ala318Pro
XM_011537475.1:c.766G>C	XP_011535777.1:p.Ala256Pro
XM_011537476.1:c.604G>C	XP_011535778.1:p.Ala202Pro
XM_011537477.1:c.913G>C	XP_011535779.1:p.Ala305Pro
XM_006719963.3:c.748G>C	XP_006720026.2:p.Ala250Pro
XM_011537474.2:c.997G>C	XP_011535776.2:p.Ala333Pro
XM_011537475.2:c.811G>C	XP_011535777.2:p.Ala271Pro
XM_011537476.2:c.604G>C	XP_011535778.1:p.Ala202Pro
NM_019616.4:c.844G>C MANE Select	NP_062562.1:p.Ala282Pro
NR_051961.2:n.928G>C
NM_001267554.2:c.658G>C	NP_001254483.1:p.Ala220Pro