Canonical Allele Identifier: CA11096025
Gene: KLF7 HGNC NCBI

Linked Data

dbSNP Id: rs2284932

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.207147785G>A , CM000664.2:g.207147785G>A GRCh38
NC_000002.11:g.208012509G>A , CM000664.1:g.208012509G>A GRCh37
NC_000002.10:g.207720754G>A NCBI36
NG_052989.1:g.24462C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000458272.2:c.102+17682C>T ENSP00000393268.1:n.102+17682C>T
ENST00000703689.1:c.102+17682C>T ENSP00000515426.1:n.102+17682C>T
ENST00000703734.1:c.102+17682C>T ENSP00000515454.1:n.102+17682C>T
ENST00000703735.1:c.102+17682C>T ENSP00000515455.1:n.102+17682C>T
ENST00000703736.1:c.3+19355C>T ENSP00000515456.1:n.3+19355C>T
ENST00000309446.11:c.102+17682C>T MANE Select ENSP00000309570.6:n.102+17682C>T
ENST00000309446.10:c.102+17682C>T ENSP00000309570.6:n.102+17682C>T
ENST00000421199.5:c.3+19355C>T ENSP00000387510.1:n.3+19355C>T
ENST00000423015.5:c.102+17682C>T ENSP00000398572.1:n.102+17682C>T
ENST00000426163.5:c.102+17682C>T ENSP00000397245.1:n.102+17682C>T
ENST00000451244.1:c.*165+1197C>T ENSP00000412950.1:n.*165+1197C>T
ENST00000457962.5:c.102+17682C>T ENSP00000392015.1:n.102+17682C>T
ENST00000458272.1:c.102+17682C>T ENSP00000393268.1:n.102+17682C>T
NM_001270942.1:c.102+17682C>T NP_001257871.1:n.102+17682C>T
NM_001270943.1:c.3+19355C>T NP_001257872.1:n.3+19355C>T
NM_003709.3:c.102+17682C>T NP_003700.1:n.102+17682C>T
NR_073108.1:n.514+17682C>T
XM_005246926.2:c.102+17682C>T XP_005246983.1:n.102+17682C>T
XM_006712815.2:c.102+17682C>T XP_006712878.1:n.102+17682C>T
XM_011512071.1:c.102+17682C>T XP_011510373.1:n.102+17682C>T
XM_011512072.1:c.102+17682C>T XP_011510374.1:n.102+17682C>T
XM_011512073.1:c.9+1197C>T XP_011510375.1:n.9+1197C>T
XM_011512074.1:c.3+19355C>T XP_011510376.1:n.3+19355C>T
XM_011512075.1:c.102+17682C>T XP_011510377.1:n.102+17682C>T
XM_011512076.1:c.102+17682C>T XP_011510378.1:n.102+17682C>T
XR_923051.1:n.523+17682C>T
XM_005246926.3:c.102+17682C>T XP_005246983.1:n.102+17682C>T
XM_006712815.3:c.102+17682C>T XP_006712878.1:n.102+17682C>T
XM_011512072.2:c.102+17682C>T XP_011510374.1:n.102+17682C>T
XM_011512073.2:c.9+1197C>T XP_011510375.1:n.9+1197C>T
XM_011512074.2:c.3+19355C>T XP_011510376.1:n.3+19355C>T
XM_011512075.2:c.102+17682C>T XP_011510377.1:n.102+17682C>T
XM_017005161.1:c.102+17682C>T XP_016860650.1:n.102+17682C>T
XM_017005163.2:c.102+17682C>T XP_016860652.1:n.102+17682C>T
XM_017005164.2:c.102+17682C>T XP_016860653.1:n.102+17682C>T
XM_024453196.1:c.3+19355C>T XP_024308964.1:n.3+19355C>T
XR_001739009.2:n.508+17682C>T
XR_923051.2:n.508+17682C>T
NM_003709.4:c.102+17682C>T MANE Select NP_003700.1:n.102+17682C>T
NM_001270943.2:c.3+19355C>T NP_001257872.1:n.3+19355C>T
NR_073108.2:n.276+17682C>T