Canonical Allele Identifier: CA425085087

Gene: KLF11

Linked Data

• MyVariant Identifiers: chr2:g.10188478T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048351T>A , CM000664.2:g.10048351T>A	GRCh38
NC_000002.11:g.10188478T>A , CM000664.1:g.10188478T>A	GRCh37
NC_000002.10:g.10105929T>A	NCBI36
NG_017199.1:g.9797T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.1014T>A MANE Select	ENSP00000307023.1:p.Ala338=
ENST00000305883.5:c.1014T>A	ENSP00000307023.1:p.Ala338=
ENST00000535335.1:c.963T>A	ENSP00000442722.1:p.Ala321=
ENST00000540845.5:c.963T>A	ENSP00000444690.1:p.Ala321=
NM_001177716.1:c.963T>A	NP_001171187.1:p.Ala321=
NM_001177718.1:c.963T>A	NP_001171189.1:p.Ala321=
NM_003597.4:c.1014T>A	NP_003588.1:p.Ala338=
XM_005246179.3:c.963T>A	XP_005246236.1:p.Ala321=
NM_003597.5:c.1014T>A MANE Select	NP_003588.1:p.Ala338=
NM_001177716.2:c.963T>A	NP_001171187.1:p.Ala321=
NM_001177718.2:c.963T>A	NP_001171189.1:p.Ala321=