Canonical Allele Identifier: CA1886882149
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781615C= , CM000672.2:g.3781615C= GRCh38
NC_000010.10:g.3823807C= , CM000672.1:g.3823807C= GRCh37
NC_000010.9:g.3813807C= NCBI36
NG_012277.1:g.8667G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.676+26G= MANE Select ENSP00000419923.1:n.676+26G=
ENST00000173785.4:n.257+180G=
ENST00000469435.1:c.702G= ENSP00000419079.1:p.Arg234=
ENST00000497571.5:c.676+26G= ENSP00000419923.1:n.676+26G=
ENST00000542957.1:c.676+26G= ENSP00000445301.1:n.676+26G=
NM_001160124.1:c.550+152G= NP_001153596.1:n.550+152G=
NM_001160125.1:c.676+26G= NP_001153597.1:n.676+26G=
NM_001300.5:c.676+26G= NP_001291.3:n.676+26G=
NR_027653.1:n.789+180G=
NM_001300.6:c.676+26G= MANE Select NP_001291.3:n.676+26G=
NM_001160124.2:c.550+152G= NP_001153596.1:n.550+152G=
NR_027653.2:n.717+180G=
NM_001160125.2:c.676+26G= NP_001153597.1:n.676+26G=