Canonical Allele Identifier: CA358945641

Gene: F11 F11-AS1

Linked Data

• gnomAD v3: 4-186287773-C-A
• gnomAD v4: 4-186287773-C-A
• MyVariant Identifiers: chr4:g.187208927C>A (hg19) ; chr4:g.186287773C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186287773C>A , CM000666.2:g.186287773C>A	GRCh38
NC_000004.11:g.187208927C>A , CM000666.1:g.187208927C>A	GRCh37
NC_000004.10:g.187445921C>A	NCBI36
NG_008051.1:g.26810C>A , LRG_583:g.26810C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.1666C>A (F11) MANE Select	ENSP00000384957.2:p.His556Asn
ENST00000264691.4:c.266C>A (F11)
ENST00000264692.8:c.1504C>A (F11)	ENSP00000264692.5:p.His502Asn
ENST00000403665.6:c.1666C>A (F11)	ENSP00000384957.2:p.His556Asn
ENST00000503841.1:n.185C>A (F11)
NM_000128.3:c.1666C>A , LRG_583t1:c.1666C>A (F11)	NP_000119.1:p.His556Asn
NR_033900.1:n.1066+655G>T (F11-AS1)
XM_005262821.2:c.1669C>A (F11)	XP_005262878.1:p.His557Asn
XM_005262822.2:c.1573C>A (F11)	XP_005262879.1:p.His525Asn
XM_005262823.2:c.1399C>A (F11)	XP_005262880.1:p.His467Asn
XM_006714137.1:c.1621C>A (F11)	XP_006714200.1:p.His541Asn
XM_005262821.4:c.1669C>A (F11)	XP_005262878.1:p.His557Asn
XM_005262822.4:c.1573C>A (F11)	XP_005262879.1:p.His525Asn
XM_005262823.4:c.1399C>A (F11)	XP_005262880.1:p.His467Asn
XM_006714137.3:c.1621C>A (F11)	XP_006714200.1:p.His541Asn
NM_000128.4:c.1666C>A (F11) MANE Select	NP_000119.1:p.His556Asn