Canonical Allele Identifier: CA358959127

Gene: F11

Linked Data

• MyVariant Identifiers: chr4:g.187197436A>C (hg19) ; chr4:g.186276282A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186276282A>C , CM000666.2:g.186276282A>C	GRCh38
NC_000004.11:g.187197436A>C , CM000666.1:g.187197436A>C	GRCh37
NC_000004.10:g.187434430A>C	NCBI36
NG_008051.1:g.15319A>C , LRG_583:g.15319A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000403665.7:c.647A>C MANE Select	ENSP00000384957.2:p.Asp216Ala
ENST00000264692.8:c.485A>C	ENSP00000264692.5:p.Asp162Ala
ENST00000403665.6:c.647A>C	ENSP00000384957.2:p.Asp216Ala
ENST00000452239.1:c.94A>C
NM_000128.3:c.647A>C , LRG_583t1:c.647A>C	NP_000119.1:p.Asp216Ala
XM_005262821.2:c.647A>C	XP_005262878.1:p.Asp216Ala
XM_005262822.2:c.647A>C	XP_005262879.1:p.Asp216Ala
XM_005262823.2:c.485+2007A>C	XP_005262880.1:n.485+2007A>C
XM_005262824.1:c.647A>C	XP_005262881.1:p.Asp216Ala
XM_006714137.1:c.647A>C	XP_006714200.1:p.Asp216Ala
XR_938706.1:n.999A>C
XR_938707.1:n.999A>C
XM_005262821.4:c.647A>C	XP_005262878.1:p.Asp216Ala
XM_005262822.4:c.647A>C	XP_005262879.1:p.Asp216Ala
XM_005262823.4:c.485+2007A>C	XP_005262880.1:n.485+2007A>C
XM_006714137.3:c.647A>C	XP_006714200.1:p.Asp216Ala
XM_017007884.2:c.647A>C	XP_016863373.1:p.Asp216Ala
XM_017007885.2:c.647A>C	XP_016863374.1:p.Asp216Ala
XM_017007886.2:c.647A>C	XP_016863375.1:p.Asp216Ala
XR_001741172.2:n.980A>C
NM_000128.4:c.647A>C MANE Select	NP_000119.1:p.Asp216Ala