Canonical Allele Identifier: CA442642058

Gene: F11 F11-AS1

Linked Data

• MyVariant Identifiers: chr4:g.187209939C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186288785C>G , CM000666.2:g.186288785C>G	GRCh38
NC_000004.11:g.187209939C>G , CM000666.1:g.187209939C>G	GRCh37
NC_000004.10:g.187446933C>G	NCBI36
NG_008051.1:g.27822C>G , LRG_583:g.27822C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403665.7:c.*171C>G (F11) MANE Select	ENSP00000384957.2:n.*171C>G
ENST00000264691.4:c.649C>G (F11)
NM_000128.3:c.*171C>G , LRG_583t1:c.*171C>G (F11)	NP_000119.1:n.*171C>G
NR_033900.1:n.709G>C (F11-AS1)
XM_005262821.2:c.*171C>G (F11)	XP_005262878.1:n.*171C>G
XM_005262822.2:c.*171C>G (F11)	XP_005262879.1:n.*171C>G
XM_005262823.2:c.*171C>G (F11)	XP_005262880.1:n.*171C>G
XM_006714137.1:c.*171C>G (F11)	XP_006714200.1:n.*171C>G
XM_005262821.4:c.*171C>G (F11)	XP_005262878.1:n.*171C>G
XM_005262822.4:c.*171C>G (F11)	XP_005262879.1:n.*171C>G
XM_005262823.4:c.*171C>G (F11)	XP_005262880.1:n.*171C>G
XM_006714137.3:c.*171C>G (F11)	XP_006714200.1:n.*171C>G
NM_000128.4:c.*171C>G (F11) MANE Select	NP_000119.1:n.*171C>G