Canonical Allele Identifier: CA468166577
Gene: KLF6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.3823924G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781732G>C , CM000672.2:g.3781732G>C GRCh38
NC_000010.10:g.3823924G>C , CM000672.1:g.3823924G>C GRCh37
NC_000010.9:g.3813924G>C NCBI36
NG_012277.1:g.8550C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000497571.6:c.585C>G MANE Select ENSP00000419923.1:p.Gly195=
ENST00000173785.4:n.257+63C>G
ENST00000469435.1:c.585C>G ENSP00000419079.1:p.Gly195=
ENST00000497571.5:c.585C>G ENSP00000419923.1:p.Gly195=
ENST00000542957.1:c.585C>G ENSP00000445301.1:p.Gly195=
NM_001160124.1:c.550+35C>G NP_001153596.1:n.550+35C>G
NM_001160125.1:c.585C>G NP_001153597.1:p.Gly195=
NM_001300.5:c.585C>G NP_001291.3:p.Gly195=
NR_027653.1:n.789+63C>G
NM_001300.6:c.585C>G MANE Select NP_001291.3:p.Gly195=
NM_001160124.2:c.550+35C>G NP_001153596.1:n.550+35C>G
NR_027653.2:n.717+63C>G
NM_001160125.2:c.585C>G NP_001153597.1:p.Gly195=