Canonical Allele Identifier: CA425084908

Gene: KLF11

Linked Data

• MyVariant Identifiers: chr2:g.10188367T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10048240T>C , CM000664.2:g.10048240T>C	GRCh38
NC_000002.11:g.10188367T>C , CM000664.1:g.10188367T>C	GRCh37
NC_000002.10:g.10105818T>C	NCBI36
NG_017199.1:g.9686T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305883.6:c.903T>C MANE Select	ENSP00000307023.1:p.Ala301=
ENST00000305883.5:c.903T>C	ENSP00000307023.1:p.Ala301=
ENST00000535335.1:c.852T>C	ENSP00000442722.1:p.Ala284=
ENST00000540845.5:c.852T>C	ENSP00000444690.1:p.Ala284=
NM_001177716.1:c.852T>C	NP_001171187.1:p.Ala284=
NM_001177718.1:c.852T>C	NP_001171189.1:p.Ala284=
NM_003597.4:c.903T>C	NP_003588.1:p.Ala301=
XM_005246179.3:c.852T>C	XP_005246236.1:p.Ala284=
NM_003597.5:c.903T>C MANE Select	NP_003588.1:p.Ala301=
NM_001177716.2:c.852T>C	NP_001171187.1:p.Ala284=
NM_001177718.2:c.852T>C	NP_001171189.1:p.Ala284=