Canonical Allele Identifier: CA2838551556

Gene: KLF12

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73761451A>G , CM000675.2:g.73761451A>G	GRCh38
NC_000013.10:g.74335588A>G , CM000675.1:g.74335588A>G	GRCh37
NC_000013.9:g.73233589A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703967.1:c.869+3487T>C MANE Select	ENSP00000515592.1:n.869+3487T>C
ENST00000377669.7:c.869+3487T>C	ENSP00000366897.2:n.869+3487T>C
ENST00000377666.5:c.794+3487T>C	ENSP00000366894.5:n.794+3487T>C
ENST00000377669.6:c.869+3487T>C	ENSP00000366897.2:n.869+3487T>C
NM_007249.4:c.869+3487T>C	NP_009180.3:n.869+3487T>C
XM_005266251.2:c.869+3487T>C	XP_005266308.1:n.869+3487T>C
XM_005266252.3:c.869+3487T>C	XP_005266309.1:n.869+3487T>C
XM_011534907.1:c.908+3487T>C	XP_011533209.1:n.908+3487T>C
XM_011534908.1:c.908+3487T>C	XP_011533210.1:n.908+3487T>C
XM_011534909.1:c.869+3487T>C	XP_011533211.1:n.869+3487T>C
XM_011534910.1:c.863+3487T>C	XP_011533212.1:n.863+3487T>C
XM_011534911.1:c.812+3487T>C	XP_011533213.1:n.812+3487T>C
XM_011534912.1:c.812+3487T>C	XP_011533214.1:n.812+3487T>C
XM_011534913.1:c.812+3487T>C	XP_011533215.1:n.812+3487T>C
XM_005266251.4:c.869+3487T>C	XP_005266308.1:n.869+3487T>C
XM_011534907.2:c.908+3487T>C	XP_011533209.1:n.908+3487T>C
XM_011534908.3:c.908+3487T>C	XP_011533210.1:n.908+3487T>C
XM_011534909.2:c.869+3487T>C	XP_011533211.1:n.869+3487T>C
XM_011534910.2:c.863+3487T>C	XP_011533212.1:n.863+3487T>C
XM_011534911.2:c.812+3487T>C	XP_011533213.1:n.812+3487T>C
XM_011534912.2:c.812+3487T>C	XP_011533214.1:n.812+3487T>C
XM_017020384.1:c.842+3487T>C	XP_016875873.1:n.842+3487T>C
XM_017020385.1:c.719+3487T>C	XP_016875874.1:n.719+3487T>C
NM_007249.5:c.869+3487T>C	NP_009180.3:n.869+3487T>C
NM_001400136.1:c.869+3487T>C MANE Select	NP_001387065.1:n.869+3487T>C
NM_001400139.1:c.869+3487T>C	NP_001387068.1:n.869+3487T>C
NM_001400141.1:c.869+3487T>C	NP_001387070.1:n.869+3487T>C
NM_001400146.1:c.869+3487T>C	NP_001387075.1:n.869+3487T>C
NM_001400147.1:c.812+3487T>C	NP_001387076.1:n.812+3487T>C
NM_001400148.1:c.812+3487T>C	NP_001387077.1:n.812+3487T>C
NM_001400149.1:c.807-45926T>C	NP_001387078.1:n.807-45926T>C
NM_001400150.1:c.779+3487T>C	NP_001387079.1:n.779+3487T>C
NM_001400151.1:c.779+3487T>C	NP_001387080.1:n.779+3487T>C
NM_001400152.1:c.869+3487T>C	NP_001387081.1:n.869+3487T>C
NM_001400153.1:c.869+3487T>C	NP_001387082.1:n.869+3487T>C