Canonical Allele Identifier: CA13833538

Gene: KLF12

Linked Data

• dbSNP Id: rs1887346
• gnomAD v2: 13-74493002-G-A
• gnomAD v3: 13-73918865-G-A
• gnomAD v4: 13-73918865-G-A
• MyVariant Identifiers: chr13:g.74493002G>A (hg19) ; chr13:g.73918865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.73918865G>A , CM000675.2:g.73918865G>A	GRCh38
NC_000013.10:g.74493002G>A , CM000675.1:g.74493002G>A	GRCh37
NC_000013.9:g.73391003G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000703967.1:c.123+25116C>T MANE Select	ENSP00000515592.1:n.123+25116C>T
ENST00000377669.7:c.123+25116C>T	ENSP00000366897.2:n.123+25116C>T
ENST00000377666.5:c.48+25116C>T	ENSP00000366894.5:n.48+25116C>T
ENST00000377669.6:c.123+25116C>T	ENSP00000366897.2:n.123+25116C>T
ENST00000472022.1:n.157+25116C>T
NM_007249.4:c.123+25116C>T	NP_009180.3:n.123+25116C>T
XM_005266251.2:c.123+25116C>T	XP_005266308.1:n.123+25116C>T
XM_005266252.3:c.123+25116C>T	XP_005266309.1:n.123+25116C>T
XM_011534907.1:c.162+25116C>T	XP_011533209.1:n.162+25116C>T
XM_011534908.1:c.162+25116C>T	XP_011533210.1:n.162+25116C>T
XM_011534909.1:c.123+25116C>T	XP_011533211.1:n.123+25116C>T
XM_011534910.1:c.117+25116C>T	XP_011533212.1:n.117+25116C>T
XM_011534911.1:c.66+25116C>T	XP_011533213.1:n.66+25116C>T
XM_011534912.1:c.66+25116C>T	XP_011533214.1:n.66+25116C>T
XM_011534913.1:c.66+25116C>T	XP_011533215.1:n.66+25116C>T
XM_005266251.4:c.123+25116C>T	XP_005266308.1:n.123+25116C>T
XM_011534907.2:c.162+25116C>T	XP_011533209.1:n.162+25116C>T
XM_011534908.3:c.162+25116C>T	XP_011533210.1:n.162+25116C>T
XM_011534909.2:c.123+25116C>T	XP_011533211.1:n.123+25116C>T
XM_011534910.2:c.117+25116C>T	XP_011533212.1:n.117+25116C>T
XM_011534911.2:c.66+25116C>T	XP_011533213.1:n.66+25116C>T
XM_011534912.2:c.66+25116C>T	XP_011533214.1:n.66+25116C>T
XM_017020384.1:c.96+25116C>T	XP_016875873.1:n.96+25116C>T
XM_017020385.1:c.-28+20225C>T	XP_016875874.1:n.-28+20225C>T
NM_007249.5:c.123+25116C>T	NP_009180.3:n.123+25116C>T
NM_001400136.1:c.123+25116C>T MANE Select	NP_001387065.1:n.123+25116C>T
NM_001400139.1:c.123+25116C>T	NP_001387068.1:n.123+25116C>T
NM_001400141.1:c.123+25116C>T	NP_001387070.1:n.123+25116C>T
NM_001400146.1:c.123+25116C>T	NP_001387075.1:n.123+25116C>T
NM_001400147.1:c.66+25116C>T	NP_001387076.1:n.66+25116C>T
NM_001400148.1:c.66+25116C>T	NP_001387077.1:n.66+25116C>T
NM_001400149.1:c.123+25116C>T	NP_001387078.1:n.123+25116C>T
NM_001400150.1:c.34-72492C>T	NP_001387079.1:n.34-72492C>T
NM_001400151.1:c.34-72492C>T	NP_001387080.1:n.34-72492C>T
NM_001400152.1:c.123+25116C>T	NP_001387081.1:n.123+25116C>T
NM_001400153.1:c.123+25116C>T	NP_001387082.1:n.123+25116C>T