Canonical Allele Identifier: CA358945977

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209647T>C (hg19) ; chr4:g.186288493T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288493T>C , CM000666.2:g.186288493T>C	GRCh38
NC_000004.11:g.187209647T>C , CM000666.1:g.187209647T>C	GRCh37
NC_000004.10:g.187446641T>C	NCBI36
NG_008051.1:g.27530T>C , LRG_583:g.27530T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1757T>C (F11) MANE Select	ENSP00000384957.2:p.Val586Ala
ENST00000264691.4:c.357T>C (F11)
ENST00000264692.8:c.1595T>C (F11)	ENSP00000264692.5:p.Val532Ala
ENST00000403665.6:c.1757T>C (F11)	ENSP00000384957.2:p.Val586Ala
ENST00000503841.1:n.276T>C (F11)
NM_000128.3:c.1757T>C , LRG_583t1:c.1757T>C (F11)	NP_000119.1:p.Val586Ala
NR_033900.1:n.1001A>G (F11-AS1)
XM_005262821.2:c.1760T>C (F11)	XP_005262878.1:p.Val587Ala
XM_005262822.2:c.1664T>C (F11)	XP_005262879.1:p.Val555Ala
XM_005262823.2:c.1490T>C (F11)	XP_005262880.1:p.Val497Ala
XM_006714137.1:c.1712T>C (F11)	XP_006714200.1:p.Val571Ala
XM_005262821.4:c.1760T>C (F11)	XP_005262878.1:p.Val587Ala
XM_005262822.4:c.1664T>C (F11)	XP_005262879.1:p.Val555Ala
XM_005262823.4:c.1490T>C (F11)	XP_005262880.1:p.Val497Ala
XM_006714137.3:c.1712T>C (F11)	XP_006714200.1:p.Val571Ala
NM_000128.4:c.1757T>C (F11) MANE Select	NP_000119.1:p.Val586Ala