Canonical Allele Identifier: CA1886882227
Gene: KLF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781801T= , CM000672.2:g.3781801T= GRCh38
NC_000010.10:g.3823993T= , CM000672.1:g.3823993T= GRCh37
NC_000010.9:g.3813993T= NCBI36
NG_012277.1:g.8481A=

Transcript Alleles

HGVS Amino-acid change
ENST00000497571.6:c.516A= MANE Select ENSP00000419923.1:p.Pro172=
ENST00000173785.4:n.251A=
ENST00000469435.1:c.516A= ENSP00000419079.1:p.Pro172=
ENST00000497571.5:c.516A= ENSP00000419923.1:p.Pro172=
ENST00000542957.1:c.516A= ENSP00000445301.1:p.Pro172=
NM_001160124.1:c.516A= NP_001153596.1:p.Pro172=
NM_001160125.1:c.516A= NP_001153597.1:p.Pro172=
NM_001300.5:c.516A= NP_001291.3:p.Pro172=
NR_027653.1:n.783A=
NM_001300.6:c.516A= MANE Select NP_001291.3:p.Pro172=
NM_001160124.2:c.516A= NP_001153596.1:p.Pro172=
NR_027653.2:n.711A=
NM_001160125.2:c.516A= NP_001153597.1:p.Pro172=