Canonical Allele Identifier: CA201345107

Gene: KLF6

Linked Data

• dbSNP Id: rs1053961825
• gnomAD v4: 10-3781586-G-T
• MyVariant Identifiers: chr10:g.3823778G>T (hg19) ; chr10:g.3781586G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.3781586G>T , CM000672.2:g.3781586G>T	GRCh38
NC_000010.10:g.3823778G>T , CM000672.1:g.3823778G>T	GRCh37
NC_000010.9:g.3813778G>T	NCBI36
NG_012277.1:g.8696C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000497571.6:c.676+55C>A MANE Select	ENSP00000419923.1:n.676+55C>A
ENST00000173785.4:n.257+209C>A
ENST00000469435.1:c.731C>A	ENSP00000419079.1:p.Ala244Glu
ENST00000497571.5:c.676+55C>A	ENSP00000419923.1:n.676+55C>A
ENST00000542957.1:c.676+55C>A	ENSP00000445301.1:n.676+55C>A
NM_001160124.1:c.550+181C>A	NP_001153596.1:n.550+181C>A
NM_001160125.1:c.676+55C>A	NP_001153597.1:n.676+55C>A
NM_001300.5:c.676+55C>A	NP_001291.3:n.676+55C>A
NR_027653.1:n.789+209C>A
NM_001300.6:c.676+55C>A MANE Select	NP_001291.3:n.676+55C>A
NM_001160124.2:c.550+181C>A	NP_001153596.1:n.550+181C>A
NR_027653.2:n.717+209C>A
NM_001160125.2:c.676+55C>A	NP_001153597.1:n.676+55C>A