Canonical Allele Identifier: CA468166775
Gene: KLF6 HGNC NCBI

Linked Data

gnomAD v4: 10-3781885-G-C
MyVariant Identifiers: chr10:g.3824077G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.3781885G>C , CM000672.2:g.3781885G>C GRCh38
NC_000010.10:g.3824077G>C , CM000672.1:g.3824077G>C GRCh37
NC_000010.9:g.3814077G>C NCBI36
NG_012277.1:g.8397C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000497571.6:c.432C>G MANE Select ENSP00000419923.1:p.Val144=
ENST00000173785.4:n.167C>G
ENST00000380946.3:n.667C>G
ENST00000469435.1:c.432C>G ENSP00000419079.1:p.Val144=
ENST00000497571.5:c.432C>G ENSP00000419923.1:p.Val144=
ENST00000542957.1:c.432C>G ENSP00000445301.1:p.Val144=
NM_001160124.1:c.432C>G NP_001153596.1:p.Val144=
NM_001160125.1:c.432C>G NP_001153597.1:p.Val144=
NM_001300.5:c.432C>G NP_001291.3:p.Val144=
NR_027653.1:n.699C>G
NM_001300.6:c.432C>G MANE Select NP_001291.3:p.Val144=
NM_001160124.2:c.432C>G NP_001153596.1:p.Val144=
NR_027653.2:n.627C>G
NM_001160125.2:c.432C>G NP_001153597.1:p.Val144=