Canonical Allele Identifier: CA358946414

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209764T>C (hg19) ; chr4:g.186288610T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288610T>C , CM000666.2:g.186288610T>C	GRCh38
NC_000004.11:g.187209764T>C , CM000666.1:g.187209764T>C	GRCh37
NC_000004.10:g.187446758T>C	NCBI36
NG_008051.1:g.27647T>C , LRG_583:g.27647T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1874T>C (F11) MANE Select	ENSP00000384957.2:p.Val625Ala
ENST00000264691.4:c.474T>C (F11)
ENST00000264692.8:c.1712T>C (F11)	ENSP00000264692.5:p.Val571Ala
ENST00000403665.6:c.1874T>C (F11)	ENSP00000384957.2:p.Val625Ala
ENST00000503841.1:n.393T>C (F11)
NM_000128.3:c.1874T>C , LRG_583t1:c.1874T>C (F11)	NP_000119.1:p.Val625Ala
NR_033900.1:n.884A>G (F11-AS1)
XM_005262821.2:c.1877T>C (F11)	XP_005262878.1:p.Val626Ala
XM_005262822.2:c.1781T>C (F11)	XP_005262879.1:p.Val594Ala
XM_005262823.2:c.1607T>C (F11)	XP_005262880.1:p.Val536Ala
XM_006714137.1:c.1829T>C (F11)	XP_006714200.1:p.Val610Ala
XM_005262821.4:c.1877T>C (F11)	XP_005262878.1:p.Val626Ala
XM_005262822.4:c.1781T>C (F11)	XP_005262879.1:p.Val594Ala
XM_005262823.4:c.1607T>C (F11)	XP_005262880.1:p.Val536Ala
XM_006714137.3:c.1829T>C (F11)	XP_006714200.1:p.Val610Ala
NM_000128.4:c.1874T>C (F11) MANE Select	NP_000119.1:p.Val625Ala